205.Perdriau S, Chang M-C, Otten E, Heeres HJ, and de Vries JG. CHEMISTRY – A EUROPEAN JOURNAL, 2014, 20, 15434-15442. Alkene Isomerisation Catalysed by a Ruthenium PNN Pincer Complex.
204.J. G. de Vries in C-1 Building Blocks in Organic Synthesis, Vol. 1, P. W. N. M. Van Leeuwen, ed., Georg Thieme Verlag AG, 2014, 1, 193-227. Hydroformylation of Alkenes: Industrial Applications.
203.J. G. de Vries, Top. Catal. 2014, 57,1306-1317. Twenty-Five Years of Homogeneous Catalysis for the Production of Bulk and Fine Chemicals: A Personal Account.
202.P. J. Deuss, K. Barta, J. G. de Vries, Catal. Sci. Technol., 2014, 4, 1174-1196. Homogeneous catalysis for the conversion of biomass and biomass-derived platform chemicals.
201.G. K. M. Verzijl, A. H. M. de Vries, J. G. de Vries, P. Kapitan, T. Dax, M. Helms, Z. Nazir, W. Skranc, C. Imboden, J. Stichler, R. A. Ward, S. Abele, L. Lefort, Org. Proc. Res. Dev., 2013, 17, 1531-1539. Catalytic Asymmetric Reduction of a 3,4-Dihydroisoquinoline for the Large-Scale Production of Almorexant: Hydrogenation or Transfer Hydrogenation?
200.J. G. de Vries, L. Lefort, Oil Gas Sci. Technol.,  2013, 68, 519-528.201. Development of Asymmetric Hydrogenation Catalysts via High Throughput Experimentation.
199.D. J. Ager, J. G. de Vries in, Transition metal-catalzyed couplings in process chemistry, J. Magano, J.R. Dunetz, eds., Wiley-VCH, Weinheim, 2013, P1-13. Copper-catalzyed coupling for a green process.
198.C. M. Nicklaus, P. H. Phua, T. Buntara, S. Noel, H. J. Heeres,  J. G. de Vries, Adv. Synth. Catal., 2013, 355, 2839-2844. Ruthenium/1,1’-Bis(diphenylphosphino)ferrocene-Catalysed Oppenauer Oxidation of Alcohols and Lactonisation of α,ω-Diols  using Methyl Isobutyl Ketone as Oxidant.
197.A. L. Gottumukkala, J. Suljagic, K. Matcha, J. G. de Vries, A. J. Minnaard, ChemSusChem 2013, 6, 1636-1639. Efficient Formation of Benzylic Quaternary Centers via Palladium Catalysis.
196.C. M. Nicklaus, A. J. Minnaard, B. L. Feringa, J. G. de Vries, ChemSusChem 2013, 6, 1631-1635. Synthesis of Renewable Fine-Chemical Building Blocks by Reductive Coupling between Furfural Derivatives and Terpenes.
195.M. Jäger, M. Hartmann, J. G. de Vries, A. J. Minnaard, Angew. Chem. Int. Ed. 2013, 52, 7809-7812. Catalytic Regioselective Oxidation of Glycosides.
194.T. Buntara, I. Melián-Cabrera, Q. Tan, J. L.G. Fierro, M. Neurock, J. G. de Vries, H. J. Heeres, Catal. Today  2013, 210, 106-116. Catalyst studies on the ring opening of tetrahydrofuran–dimethanol to 1,2,6-hexanetriol.
193.R.-J. van Putten, J. C. van der Waal, E. de Jong, C. B. Rasrendra, Hero J. Heeres, J. G. de Vries, Chem. Rev. 2013, 113, 1499−1597. Hydroxymethylfurfural, A Versatile Platform Chemical Made from Renewable Resources.
192.S. Perdriau, S. Harder, H. J. Heeres, J. G. de Vries, ChemSusChem,  2012, 5, 2427-2434. Selective Conversion of Polyenes to Monoenes by RuCl3-Catalyzed Transfer Hydrogenation : The Case of Cashew Nutshell Liquid.
191.C. Sole, A. Bonet, A. H. M. de Vries, J. G. de Vries, L. Lefort, H. Gulyás, E. Fernández, Organometallics 2012, 31, 7855−7861. Influence of Phosphoramidites in Copper-Catalyzed Conjugate Borylation Reaction.
190.L. Lefort, N. Sereinig, H. Straatman, D. J. Ager, J. G. de Vries, J. A. Werner, R. B. Scherer, T. D. Maloney, M. D. Argentine, K. A. Sullivan J. W. Fennell, Catal. Sci. Technol., 2012, 2, 2077-2082. A detailed study of the diastereoselective catalytic hydrogenation of 6-hydroxytetrahydroisoquinoline-(3R)-carboxylic ester intermediates.
189.J. G. de Vries, S. D. Jackson, Catal. Sci. Technol., 2012, 2, 2009-2009. Homogeneous and Heterogeneous Catalysis in Industry.
188.D. J. Ager, J. G. de Vries in Comprehensive Chirality, E. M. Carreira, H. Yamamoto, Eds., Elsevier, Amsterdam, 2012, Vol 9, D. L. Hughes, ed.,  p73-82. Industrial Applications of Asymmetric Reduction of C=C Bonds.
187.J. G. de Vries, in Organometallics as Catalysts in the Fine Chemical Industry, M. Beller, H.-U. Blaser, eds., Top. Organomet. Chem. 2012, 42, 1-34. Palladium-Catalysed Coupling Reactions.
186.P. C. J. Kamer, P. W. N. M. van Leeuwen, eds., John Wiley & Sons, Ltd., Chichester, 2012, p 133-157. Phosphoramidite Ligands. L. Lefort and J. G. de Vries in Phosphorus(III) Ligands in Homogeneous Catalysis. Design and Synthesis.
185.T. Buntara, S. Noel, P. H. Phua, I. Melián-Cabrera, J. G. de Vries, H. J. Heeres, Top. Catal. 2012, 55, 612-619. From 5-Hydroxymethylfurfural (HMF) to Polymer Precursors: Catalyst Screening Studies on the Conversion of 1,2,6-hexanetriol to 1,6-hexanediol.
184.A. L. Gottumukkala, K. Matcha, M. Lutz, J. G. de Vries, A. J. Minnaard, Chem. Eur. J. 2012, 18, 6907-6914. Palladium-Catalyzed Asymmetric Quaternary Stereocenter Formation.
183.D. J. Ager, A. H. M. de Vries J. G. de Vries, Chem. Soc. Rev., 2012, 41, 3340–3380. Asymmetric homogeneous hydrogenations at scale.
182.D. L. Dodds, M. D. K. Boele, G. P. F. van Strijdonck, J. G. de Vries, P. W. N. M. van Leeuwen, P. C. J. Kamer, Eur. J. Inorg. Chem. 2012, 1660-1671. Design, Testing and Kinetic Analysis of Bulky Monodentate Phosphorus Ligands in the Mizoroki–Heck Reaction.
181.N. Pannetier, J.-B. Sortais, J.-T. Issenhuth, L. Barloy, C. Sirlin, A. Holuigue, L. Lefort, L. Panella, J. G. de Vries, M. Pfeffer, Adv. Synth. Catal. 2011, 353, 2844-2852. Cyclometalated Complexes of Ruthenium, Rhodium and Iridium as Catalysts for Transfer Hydrogenation of Ketones and Imines.
180.E. Alberico, W. Baumann, J. G. de Vries, H.-J. Drexler, S. Gladiali, D. Heller, H. J. W. Henderickx, L. Lefort, Chem. Eur. J. 2011, 17, 12683-12695. Unravelling the Reaction Path of Rhodium–MonoPhos-Catalysed Olefin Hydrogenation.
179.T. Buntara, S. Noel, P. H. Phua, I. Melián-Cabrera, J. G. de Vries and H. J. Heeres, Angew. Chem. Int. Ed. 2011, 50, 7083-7087. Caprolactam from Renewable Resources: Catalytic Conversion of 5-Hydroxymethylfurfural into Caprolactone.
178.J. G. de Vries, N. Mršić, Catal. Sci. Technol., 2011, 1, 727–735. Organocatalytic asymmetric transfer hydrogenation of imines.
177.J. G. de Vries in Selective Nanocatalysts and Nanoscience, A. Zecchina, S. Bordiga, E. Groppo, Eds., Wiley-VCH, Weinheim, 2011. p73-104. When does catalysis with transition metal complexes turn into catalysis by nanoparticles?
176.N. Mršić, L. Panella, E. G. IJpeij, A. J. Minnaard, B. L. Feringa, J. G. de Vries, ChemCatChem, 2011, 3, 1139 -1142. Methylaluminoxane as an Alternative for BArF in the Iridium-Catalyzed Asymmetric Hydrogenation of Imines.
175.J. G. de Vries, A. J. Minnaard, Chem. Eur. J. 2011, 17, 3091 – 3095. Pd–NHC Catalyzed Conjugate Addition versus the Mizoroki–Heck Reaction. A. L. Gottumukkala.
174.N. Mršić, L. Panella, A. J. Minnaard, B. L. Feringa, J. G. de Vries, Tetrahedron: Asymmetry 2011, 22, 36–39. Synthesis of N-phenyl β-amino acids via iridium-catalyzed asymmetric hydrogenation using mixed monodentate ligands.
173.B. de Lange, D. J. Hyett, P. J. D. Maas, D. Mink, F. B. J. van Assema, N. Sereinig, A. H. M. de Vries and Johannes G. de Vries, ChemCatChem 2011, 3, 289 – 292. Asymmetric Synthesis of (S)-2-Indolinecarboxylic Acid by Combining Biocatalysis and Homogeneous Catalysis.
172.B. J. V. Verkuijl, J. G. de Vries, B. J. Feringa, Chirality, 2011, 23, 34–43. 3,3’-Diaryl-BINOL Phosphoric Acids as Enantioselective Extractants of Benzylic Primary Amines.
171.Boelo Schuur, Bastiaan J. V. Verkuijl, Adriaan J. Minnaard, Johannes G. de Vries, Hero J. Heeres and Ben L. Feringa, Org. Biomol. Chem., 20119, 36-51. Chiral separation by enantioselective liquid–liquid extraction.
170.B. Schuur, B. J. V. Verkuijl, J. Bokhove, A. J. Minnaard, J. G. de Vries, H. J. Heeres, B. L. Feringa Tetrahedron, 2011, 67, 462-470. Enantioselective liquid/liquid extraction of (R,S)-phenylglycinol using a bisnaphthyl phosphoric acid derivative as chiral extractant.
169.E. Sperotto, G. P.M. van Klink, J. G. de Vries, G. van Koten, Tetrahedron, 2010, 66, 9009-9020. Aminoarenethiolato-copper(I) as (pre-)catalyst for the synthesis of diaryl ethers from aryl bromides and sequential C–O/C–S and C–N/C–S cross coupling reactions.
168.E. Sperotto, G. P. M. van Klink, G. van Koten, J. G. de Vries, Dalton Trans., 2010, 39, 10338–10351. The mechanism of the modified Ullmann reaction.
167.T. Orbegozo, J. G. de Vries, W. Kroutil, Eur. J. Org. Chem. 2010, 3445–3448. Biooxidation of Primary Alcohols to Aldehydes through Hydrogen Transfer Employing Janibacter terrae.
166.B. J. V. Verkuijl, A. K.  Schoonen, A. J. Minnaard, J. G. de Vries, B. L. Feringa, Eur. J. Org. Chem. 2010, 5197–5202. The Use of N-Type Ligands in the Enantioselective Liquid–Liquid Extraction of Underivatized Amino Acids.
165.B. Stegink, L. van Boxtel, L. Lefort, A. J. Minnaard,B. L. Feringa, J. G. de Vries, Adv. Synth. Catal. 2010, 352, 2621 – 2628. Ruthenium-Catalysed Hydrogenation of Aromatic Ketones using Monodentate Phosphoramidite Ligands.
164.F. G. Mutti, A. Orthaber, J. H. Schrittwieser, J. G. de Vries, R. Pietschnig and W. Kroutil, Chem. Commun., 2010, 46, 8046-8048. Simultaneous iridium catalysed oxidation and enzymatic reduction employing orthogonal reagents.
163.W. Szymanski, C. P. Postema, C. Tarabiono, F. Berthiol,L. Campbell-Verduyn, S. de Wildeman, J. G. de Vries, B. L. Feringa, D. B. Janssen, Adv. Synth. Catal. 2010, 352, 2111-2115. Combining Designer Cells and Click Chemistry for a One-Pot Four-Step Preparation of Enantiopure b-Hydroxytriazoles.
162.G. C. Lloyd-Jones,  A. J. Robinson, L. Lefort, J. G. de Vries, Chem. Eur. J. 2010, 16, 9449 – 9452. A Simple and Effective Co-Catalyst for Ring-Closing Enyne Metathesis Using Grubbs I type Catalysts: A Practical Alternative to “Mori’s Conditions”.
161.C. Rangheard, C. de Julián Fernández, P.-H. Phua, J. Hoorn, L. Lefort and J. G. de Vries, Dalton Trans., 2010, 39, 8464–8471. At the frontier between heterogeneous and homogeneous catalysis: hydrogenation of olefins and alkynes with soluble iron nanoparticles.
160.G. F. Busscher, L. Lefort, J. G. O. Cremers , M. Mottinelli, R. W. Wiertz, B. de Lange, Y. Okamura, Y. Yusa, K. Matsumura, H. Shimizu, J. G. de Vries, A. H. M. de Vries. Tetrahedron: Asymmetry, 2010, 21, 1709–1714. Efficient preparation of an N-aryl b-amino acid via asymmetric hydrogenation and direct asymmetric reductive amination en route to Ezetimibe.
159.T. Orbegozo, J. G. de Vries, W. Kroutil, Eur. J. Org. Chem. 2010, 3445–3448. Biooxidation of Primary Alcohols to Aldehydes through Hydrogen Transfer Employing Janibacter terrae.
158.L. Lefort, J. A. F. Boogers, J. G. de Vries, A. H. M. de Vries, Top. Catal. 2010, 53, 1081-1086. Under Pressure: Rapid Development of Scalable Asymmetric Hydrogenation Catalysts.
157.T. Jerphagnon, R. Haak,  F. Berthiol, A. J. A. Gayet, V. Ritleng, A. Holuigue, N. Pannetier, M. Pfeffer, A. Voelklin, L. Lefort, G. Verzijl, C. Tarabiono, D. B. Janssen, A. J. Minnaard, B. L. Feringa,  J. G. de Vries, Top Catal. 2010, 53, 1002–1008. Ruthenacycles and Iridacycles as Catalysts for Asymmetric Transfer Hydrogenation and Racemisation.
156.B. Schuur, J. G. M. Winkelman, J. G. de Vries, H. J. Heeres, Chem. Eng. Sci. 2010, 65  4682–4690. Experimental and modeling studies on the enantio-separation of 3,5-dinitrobenzoyl-(R),(S)-leucine by continuous liquid–liquid extraction in a cascade of centrifugal contactor separators.
155.B. J. V. Verkuijl, B. Schuur, A. J. Minnaard, J. G. de Vries, B. L. Feringa, Org. Biomol. Chem., 2010, 8, 3045 – 3054. Chiral separation of substituted phenylalanine analogues using chiral palladium phosphine complexes with enantioselective liquid–liquid extraction.
154.E. Sperotto, G. P.M. van Klink, J. G. de Vries, G. van Koten, Tetrahedron 2010, 663478–3484. C–N Coupling of nitrogen nucleophiles with aryl and heteroaryl bromides usingaminoarenethiolato–copper(I) (pre-)catalyst.
153.L. Lefort, J. A. F. Boogers, T. Kuilman, R.-J Vijn, J. Janssen, H. Straatman, J. G. de Vries, and A. H. M. de Vries, Org. Proc. Res. Dev. 2010, 14, 568–573. Rapid Identification of a Scalable Catalyst for the Asymmetric Hydrogenation of a Sterically Demanding Aryl Enamide.
152.J. A. F. Boogers, D. Sartor, U. Felfer, M. Kotthaus, G. Steinbauer, B. Dielemans, L. Lefort, A. H. M. de Vries, and J. G. de Vries in Asymmetric Catalysis on Industrial Scale. Challenges, Approaches and Solutions, 2nd ed. H.-U. Blaser, H.-J. Federsel, Eds., Wiley-VCH, Weinheim, 2010, p 127-150. Asymmetric Hydrogenation of a 2-isopropylcinnamic acid derivative en route to the blood pressure lowering agent Aliskiren.
151.N. Mršić, T. Jerphagnon, A. J. Minnaard, B. L. Feringa, J. G. de Vries, Tetrahedron: Asymmetry, 2010, 21, 7-10. Asymmetric hydrogenation of 2-substituted N-protected-indoles catalyzed by rhodium complexes of BINOL-derived phosphoramidites.
150.B. J.  V. Verkuijl,  W. Szymański, B. Wu, A. J. Minnaard, D. B. Janssen, J. G. de Vries and B. L. Feringa, Chem. Commun., 2010, 901-903. Enantiomerically pure b-phenylalanine analogues from α,β-phenylalanine mixtures in a single reactive extraction step.
149.V. F. Slagt, A. H. M. de Vries, J. G. de Vries and R. M. Kellogg, Org. Proc. Res. Dev. 2010, 14, 30–47. Practical Aspects of Carbon-Carbon Cross-Coupling Reactions Using Heteroarenes.
148.B. Schuur, M. Steensma, J. G. M. Winkelman, J. G. de Vries, A. B. de Haan, H. J. Heeres, Chimica Oggi, 2009, 27 (6), Supplement on chiral technologies p9-12. Continuous enantioseparation by liquid-liquid extraction.
147.T. Jerphagnon, A. J. A. Gayet, F. Berthiol, V. Ritleng, N. Mršić, A. Meetsma, M. Pfeffer, A. J. Minnaard, B. L. Feringa, J. G. de Vries,  Chem. Eur. J. 2009, 15, 12780 – 12790. Fast Racemisation of Chiral Amines and Alcohols by Using Cationic Half-Sandwich Ruthena- and Iridacycle Catalysts.
146.Iridium/PipPhos, N. Mršić, T. Jerphagnon, A. J. Minnaard, B. L. Feringa and J. G. de Vries, Adv. Synth. Catal, 2009, 351, 2549-2552. Asymmetric Hydrogenation of Quinoxalines Catalyzed.
145.B. H. G. Swennenhuis, R. Chen, P. W. N. M. van Leeuwen, J. G. de Vries and P. C. J. Kamer, Eur. J. Org. Chem., 2009, 5796-5803. Supported Chiral Monodentate Ligands in Rhodium-Catalysed Asymmetric Hydrogenation and Palladium-Catalysed Asymmetric Allylic Alkylation.
144.B. Schuur, A. J. Hallett, J. G. M. Winkelman, J. G. de Vries, and H. J. Heeres, Org. Proc. Res. Dev. 2009, 13, 911–914. Scalable Enantioseparation of Amino Acid Derivatives Using Continuous Liquid-Liquid Extraction in a Cascade of Centrifugal Contactor Separators.
143.B. J. V. Verkuijl, A. J. Minnaard, J. G. de Vries and B. L. Feringa, J. Org. Chem. 2009, 74, 6526–6533. Chiral Separation of Underivatized Amino Acids by Reactive Extraction with Palladium-BINAP Complexes.
142.T. Orbegozo, I. Lavandera, W. M. F. Fabian, B. Mautner, J. G. de Vries, W. Kroutil, Tetrahedron, 2009, 65, 6805-6809. Biocatalytic oxidation of benzyl alcohol to benzaldehyde via hydrogen transfer.
141.P. H. Phua, L. Lefort, J. A. F. Boogers, M. Tristany and J. G. de Vries, Chem. Commun. 2009, 3747-3749. Soluble iron nanoparticles as cheap and environmentally benign alkene and alkyne hydrogenation catalysts.
140.D. J. Ager, L. Lefort and J. G. de Vries in Asymmetric Synthesis and Application of α-Amino Acids, V. A. Soloshonok, K. Izawa, eds., ACS Symposium Series, 1009, Oxford University Press, Oxford, 2009, Chapter 15, p239-250. Catalyst screening for the synthesis of amino acids.
139.N. Mršić, A. J. Minnaard, B. L. Feringa and J. G. de Vries, J. Am. Chem. Soc., 2009, 131, 8358-8359. Iridium/Monodentate Phosphoramidite Catalyzed Asymmetric Hydrogenation of N-Aryl Imines.
138.A. J. Hallett, G. J. Kwant, J. G. de Vries, Chem. Eur. J., 2009, 15, 2111-2120. Continuous Separation of Racemic 3,5-Dinitrobenzoyl-Amino acids in a Centrifugal Contact Separator with the aid of Cinchona-Based Chiral Host Compounds.
137.G. N. Kraai, B. Schuur, F. van Zwol, R. M. Haak, A. J. Minnaard, B. L. Feringa, H. J. Heeres and J. G. de Vries in Chemical Industries 123, Catalysis of Organic Reactions, M. L. Prunier, Ed., CRC Press, Boca Raton, 2009, p39-49. Process intensification. Continuous Two-Phase Catalytic reactions in a Table-Top Centrifugal Contact Separator.
136.R. M. Haak, F. Berthiol, T. Jerphagnon, A. J. A. Gayet, C. Tarabiono, C. P. Postema, V. Ritleng, M. Pfeffer, D. B. Janssen, A. J. Minnaard, B. L. Feringa, J. G. de Vries, J. Am. Chem. Soc., 2008, 130, 13508-13509. Dynamic Kinetic Resolution of Racemic β-Haloalcohols: Direct Access to Enantioenriched Epoxides.
135.D. J. Ager and J. G. de Vries, Chim. Oggi. 2008, 26 (5), Supplement : Focus on Chiral Technologies, p10-11. From monodentate to bidentate to monodentate with a trillion possibilities.
134.B. Schuur, J. Floure, A. J. Hallett, J. G. M. Winkelman, J. G. de Vries, and H. J. Heeres, Org. Proc. Res. Dev. 2008, 12, 950 – 955. Continuous Chiral Separation of Amino Acid Derivatives by Enantioselective Liquid-Liquid Extraction in Centrifugal Contactor Separators.
133.G. N. Kraai, J. G. M. Winkelman, J. G. de Vries, H. J. Heeres, Biochem. Eng. J.,  2008,  41, 87–94. Kinetic studies on the Rhizomucor miehei lipase catalyzed esterification reaction of oleic acid with 1-butanol in a biphasic system.
132.R. den Heeten, B. H. G. Swennenhuis, P. W. N. M. van Leeuwen, J. G. de Vries, P.  C. J. Kamer, Angew. Chem. Int. Ed. 2008, 47, 6602 –6605. Parallel Synthesis and Screening of Polymer-Supported Phosphorus-Stereogenic Aminophosphane–Phosphite and –Phosphinite Ligands.
131.E. Sperotto, G. P. M. van Klink, J. G. de Vries, G. van Koten, J. Org. Chem., 2008, 73, 5625-5628. Ligand-Free Copper-Catalyzed C−S Coupling of Aryl Iodides and Thiols.
130.L. Lefort, J. A. F. Boogers, A. H. M. de Vries, D. J. Ager, R. B. C. Jagt, A. J. Minnaard, B. L. Feringa, J. G. de Vries, Chimica Oggi, 2008, 26 (2), 26-27. MonoPhosTM is really TrillionPhos.
129.G. N. Kraai, F. van Zwol, B. Schuur, H. J. Heeres and J. G. de Vries, Angew. Chem. Int. Ed., 2008, 47, 3905-3908. Two-Phase (Bio)Catalytic Reactions in a Table-Top Centrifugal Contact Separator.
128.N. Mršić, L. Lefort, J. A. F. Boogers, A. J. Minnaard, B. L. Feringa and J. G. de Vries, Adv. Synth. Catal., 2008, 350, 1081-1089. Asymmetric Hydrogenation of Quinolines Catalyzed by Iridium Complexes of Monodentate BINOL-Derived Phosphoramidites.
127.L. Lefort and J. G. de Vries in Phosphorus Ligands in Asymmetric Catalysis, ed. A. Börner, Wiley-VCH, 2008, Vol. 3, p1348-1376. Parallel Synthesis of Chiral P-Ligands.
126.B. H. G. Swennenhuis, R. Chen, P. W. N. M. van Leeuwen, J. G. de Vries, and P. C. J. Kamer, Org. Lett., 2008, 10, 989-992. Solid-phase parallel synthesis of phosphite ligands.
125.D. J. Ager, O. May, J. G. de Vries, Chimica Oggi, 2008, 26 (1), 6-7. In search of catalysts: making the trillion to one bet pay off.
124.L. Djakovitch, K. Köhler and J. G. de Vries, In Nanoparticles and Catalysis, D. Astruc, ed., Wiley-VCH, 2008, p303-348. The role of palladium nanoparticles as catalysts for carbon-carbon coupling reactions.
123.K. F. W. Hekking, L. Lefort, A. H. M. de Vries, F. L. van Delft, H. E. Schoemaker, J. G. de Vries and F. P. J. T. Rutjes, Adv. Synth. Catal., 2008, 350, 85-94. Synthesis of Versatile Building Blocks through Asymmetric Hydrogenation of Functionalized Itaconic Acid Mono-Esters.
122.A. F. Meindertsma, M. M. Pollard, B. L. Feringa, J. G. de Vries and A. J. Minnaard, Tetrahedron:Asymmetry,  2007, 18, 2849-2858. Asymmetric hydrogenation of alkyl(vinyl)thioethers: a promising approach to α-chiral thioethers.
121.A. J. Minnaard, B. L. Feringa, L. Lefort and J.G. de Vries, Acc. Chem. Res., 2007, 40, 1267-1277. Asymmetric Hydrogenation using Monodentate Phosphoramidite Ligands.
120.E. Sperotto, J. G. de Vries, G. P. M. van Klink, G. van Koten, Tetrahedron Lett., 2007, 48, 7366-7370. Ligand-free copper(I) catalyzed N- and O-arylation of aryl halides.
119.D. J. Ager and J. G. de Vries, Speciality Chemicals 2007 (Sept.) 24. MonoPhos Ligands: More than asymmetric hydrogenation.
118.D.J. Ager, A. H. M. de Vries and J. G. de Vries, Chimica Oggi, 2007, 25 (4), 35-36. A little of this and none of that.
117.R. B. C. Jagt, P. Y. Toullec, E. P. Schudde, J. G. de Vries, B. L. Feringa and A. J. Minnaard, J. Comb. Chem.,  2007, 9, 407-414. Synthesis of solution-phase phosphoramidite and phosphite ligand libraries and their in situ screening in the rhodium-catalyzed asymmetric addition of arylboronic acids.
116.P. Huat Phua, S. P. Mathew, A. J. P. White, J. G. de Vries, D. G. Blackmond and K. K. Hii, Chem. Eur. J., 2007, 13, 4602-4613. Elucidating the mechanism of the asymmetric aza-Michael reaction.
115.R. Imbos, J.-G. Boiteau, A. Duursma, J. A. F. Boogers, A. H. M. De Vries, D. Ager, R. B. C. Jagt, A.J. Minnaard, B. L. Feringa and J. G. de Vries, Chimica Oggi, 2007, 25(2), Supplement on Catalysis Applications, 18-19. Catalysts for this; Catalysts for that: now, Rhodium-MonoPhosTM for asymmetric C-C bond formation.
114.J. A. F. Boogers, U. Felfer, M. Kotthaus, L. Lefort, G. Steinbauer, A. H. M. de Vries, and J. G. de Vries. Org. Proc. Res. Dev., 2007, 11, 585-591. A mixed ligand approach enables the asymmetric hydrogenation of an alpha-isopropyl-cinnamic acid en route to the renin-inhibitor Aliskiren.
113.E. L. Myers, J. G., de Vries and V. Aggarwal, Angew,. Chem. Int. Ed., 2007, 46, 1893-1896. Reactions of iminium ions with Michael acceptors through a Morita-Baylis-Hillman-type reaction: Enantiocontrol and applications in synthesis.
112.F. Giacomina, A. Meetsma, L. Panella, L. Lefort, A. H. M. de Vries and J. G. de Vries, Angew. Chem. Int. Ed., 2007, 46, 1497-1500. High Enantioselectivity Is Induced by a Single Monodentate Phosphoramidite Ligand in Iridium-Catalyzed Asymmetric Hydrogenation.
111.R. M. Haak, C. Tarabiono, D. B. Janssen, A. J. Minnaard, J. G. de Vries and B. L. Feringa, Org. Biomol. Chem., 2007, 5, 318-323. Synthesis of enantiopure chloroalcohols by enzymatic kinetic resolution.
110.R. Hoen, T. Tiemersma-Wegman, B. Procuranti, L. Lefort, J. G. de Vries, A. J. Minnaard and B. L. Feringa, Org. Biomol. Chem.,  2007, 5, 267-275. Enantioselective synthesis of β2-amino acids using rhodium-catalyzed hydrogenation.
109.D. Heller, A. H. M. de Vries and J. G. de Vries in The Handbook of Homogeneous Hydrogenation, J. G. de Vries and C. J. Elsevier, eds., Wiley-VCH, Weinheim, 2007, Vol 3, 1483-1516. Catalyst Inhibition and Deactivation in Homogeneous Hydrogenation.
108.J. G. de Vries and L. Lefort in The Handbook of Homogeneous Hydrogenation, J. G. de Vries and C. J. Elsevier, eds., Wiley-VCH, Weinheim, 2007, Vol 3, p1248-1278. High-throughput Experimentation and Ligand Libraries.
107.L. Lefort, J. A.F. Boogers, A. H.M. de Vries, and J. G. de Vries, Topics Catal., 2006, 40 (1-4), 185-191. High throughput screening of Monophos instant ligand library leads to a ton-scale asymmetric hydrogenation process.
106.A. Baber, J. G. de Vries, A. G. Orpen, P. G. Pringle, K. von der Luhe. Dalton Trans., 2006, 4821-4828. Allosteric effects in asymmetric hydrogenation catalysis? Asymmetric induction as a function of the substrate and the backbone flexibility of C-1 symmetric diphosphines in rhodium-catalysed hydrogenations.
105.S. L. X. Martina, R. B. C. Jagt, J. G. de Vries, B. L. Feringa and A. J. Minnaard, Chem. Commun., 2006, 4093-4095. Enantioselective rhodium-catalyzed addition of arylboronic acids to trifluoromethylketones.
104.B. de Lange, M. H. Lambers-Verstappen, L. Schmieder-van de Vondervoort, N. Sereinig, R. de Rijk, A. H. M. de Vries, J. G. de Vries, Synlett, 2006, 3105. Aromatic Amination of Aryl Bromides Catalysed by Copper/β-Diketone Catalysts: The Effect of Concentration.
103.P. Y. Toullec, R. B. C. Jagt, J. G. de Vries, B. L. Feringa, A. J. Minnaard, Org. Lett., 2006,  8, 2715-2718. Rhodium-Catalyzed Addition of Arylboronic Acids to Isatins: An Entry to Diversity in 3-Aryl-3-Hydroxyoxindoles.
102.J. G. de Vries and L. Lefort, Chem. Eur. J., 2006, 12, 4722-4734. The Combinatorial Approach to Asymmetric Hydrogenation: Phosphoramidite Libraries, Ruthenacycles and Artificial Enzymes.
101.R. V. Wisman, J. G. de Vries, B.-J. Deelman and H. J. Heeres, Org. Proc. Res. Dev., 2006, 10, 423-429. Kinetic studies on the asymmetric transfer hydrogenation of acetophenone using a homogeneous ruthenium catalyst with a chiral amino-alcohol ligand.
100.D. J. Ager, A. H. M de Vries and J. G. de Vries Platinum Metals Rev. 2006, 50(2), 54-63. Phosphoramidite-Controlled Asymmetric Hydrogenation with Rhodium Catalysts.
99.R. B. Jagt, P. Y. Toullec, D. Geerdink, J. G. de Vries, B. L. Feringa and A. J. Minnaard, Angew. Chem. Int. Ed., 2006, 45, 2789-2791. A Ligand-Library Approach to the Highly Efficient Rhodium/Phosphoramidite-Catalyzed Asymmetric Arylation of N, N-Dimethyl-sulfamoyl-Protected Aldimines.
98.J.-B. Sortais, L. Barloy, C. Sirlin, A. H. M. de Vries, J. G. de Vries, and M. Pfeffer, Pure Appl. Chem., 2006, 78, 457-462. Cycloruthenated compounds as efficient catalyst for asymmetric hydride transfer reaction.
97.T. B. Reeve, J.-P. Cros, C. Gennari, U. Piarulli, and J. G. de Vries, Angew. Chem. Int. Ed., 2006, 45, 2449–2453. A Practical Approach to the Resolution of Racemic N-Benzyl a-Amino Acids by Liquid–Liquid Extraction with a Lipophilic Chiral Salen–Cobalt(III) Complex.
96.R. B. C. Jagt, P. Y. Toullec, J. G. de Vries, B. L. Feringa and A. J. Minnaard, Org. Bio. Chem., 2006, 4, 773-775. Rhodium/phosphoramidite-catalyzed asymmetric arylation of aldehydes with arylboronic acids.
95.L. Panella, A. M. Aleixandre, G. J. Kruidhof, J. Robertus, B. L.  Feringa, J. G. de Vries and A. J.  Minnaard, J. Org. Chem., 2006, 71, 2026-2036. Enantioselective Rh-Catalyzed Hydrogenation of N-Formyl Dehydroamino Esters with Monodentate Phosphoramidite Ligands.
94.P. H. Phua, A. J. P. White, J. G. de Vries and K. K. Hii, Adv. Synth. Catal., 2006, 348, 587-592. Enabling Ligand Screening for Palladium-Catalysed Enantioselective Aza-Michael Addition Reactions.
93.X.- B. Jiang, L. Lefort, P. E. Goudriaan, A. H. M. de Vries, P. W. N. M. van Leeuwen, J. G. de Vries, and J. N.H. Reek, Angew. Chem. Int. Ed.,  2006, 45, 1223-1227. Screening of a Supramolecular Catalyst Library in the Search for Selective Catalysts for the Asymmetric Hydrogenation of a Difficult Enamide Substrate.
92.J. G. de Vries, Dalton Trans., 2006, 421-429. A unifying mechanism for all high-temperature Heck reactions. The role of palladium colloids and anionic species.
91.J. G. de Vries in Handbook of Chiral Chemicals, 2nd edition, D. J. Ager, Ed., CRC Press, Boca Raton. Asymmetric Olefin Hydrogenation Using Monodentate BINOL- and Bisphenol-Based Ligands: Phosphonites, Phosphites, and Phosphoramidites; 2005, p269-286.
90.T. Jerphagnon, G. P. M. van Klink, J. G. de Vries and G. van Koten,  Org. Lett., 2005,  7, 5241-5244. Aminoarenethiolate-Copper(I)-Catalyzed Amination of Aryl Bromides.
89.J. Christoffers and A. Baro, eds. Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2005, p25-50. Important pharmaceuticals and intermediates, J. G. de Vries in Quaternary Stereocenters. Challenges and Solutions for Organic Synthesis.
88.P. H. Phua, J. G. de Vries and K. K. Hii, Adv. Synth. Catal, 2005, 347, 1775-80. Palladium-catalysed enantioselective conjugate addition of aromatic amines to α,β-unsaturated N-imides. Effect of the chelating moiety.
87.G. C. Lloyd-Jones, R. G. Margue and J. G. de Vries, Angew. Chem. Int. Ed., 2005, 44, 7442-7. Rate enhancement by ethylene in the Ru-catalyzed ring-closing metathesis of enynes: Evidence for an “Ene-then-yne” pathway that diverts through a second catalytic cycle.
86.J. G. de Vries, Fudan Xuebao, Ziran Kexueban, 2005, 44(5), 829-830. The combinatorial approach to asymmetric hydrogenation: More miles out of MonoPhos.
85.L. Panella, J. Broos, J. Jin, M. W. Fraaije, D. B. Janssen, M. Jeronimus-Stratingh, B. L. Feringa, A. J. Minnaard and J. G. de Vries, Chem. Commun., 2005, 5656-5658. Merging homogeneous catalysis with biocatalysis. Papain as hydrogenation catalyst.
84.C. Gennari, C. Monti, U. Piarulli, J. G. de Vries, A. H. M. de Vries, L. Lefort, Chem. Eur. J.  2005, 11, 6701-6717. Rh-catalysed asymmetric hydrogenation of prochiral olefins with a dynamic library of chiral tropos phosphorus ligands.
83.P. W. N. M. van Leeuwen and J. G. de Vries in Handbook of C-H transformations, G. Dyker. ed., Wiley-VCH, Weinheim, 2005, Vol 1, p203-212. Palladium-catalyzed oxidative vinylation.
82.L. Panella, B. L. Feringa, J. G. de Vries and A. J. Minnaard, Org. Lett., 2005,  7, 4177-4180. Enantioselective Rh-catalyzed hydrogenation of enol acetates and enol carbamates with monodentate phosphoramidites.
81.R. B. C. Jagt, J. G. de Vries, B. L. Feringa and A. J. Minnaard, Org. Lett., 2005, 7, 2433-2435. Enantioselective synthesis of 2-aryl-4-piperidones via rhodium/phosphoramidite-catalyzed conjugate addition of boroxines.
80.R. Hoen, J. A. F. Boogers, H. Bernsmann, A. J. Minnaard, A. Meetsma, T. D. Tiemersma-Wegman, A. H. M. de Vries, J. G. de Vries, B. L. Feringa, Angew, Chem. In. Ed., 2005, 44 (27), 4209-4212. Achiral Ligands Dramatically Enhance Rate and Enantioselectivity in the Rh/Phosphoramidite-Catalyzed Hydrogenation of α,β-Disubstituted Unsaturated Acids.
79.D. J. Ager, A. H. M. de Vries and J. G. de Vries, Spec. Chem. Mag. 2005, 25 (5), 30-31. Metal-catalysed reactions: Less can be better.
78.Instant ligand libraries beat the time-to-market constraint. A. H. M. de Vries, L. Lefort, J. A. F. Boogers, J. G. de Vries and D. J. Ager, Chimica Oggi, 2005, 23(2), Supplement on Chiral Technologies, 18-22.
77.G. K. M. Verzijl, J. G. de Vries and Q. B. Broxterman, Tetrahedron Asymm., 2005, 16, 1603-1610. Removal of the acyl donor residue allows the use of simple alkyl esters as acyl donor for the dynamic kinetic resolution of secondary alcohols.
76.J.-B. Sortais, V. Ritleng, A. Voelklin, A. Holuigue, H. Smail, L. Barloy, C. Sirlin, G. K. M. Verzijl, J. A. F. Boogers, A. H. M. de Vries, J. G. de Vries and M. Pfeffer, Org. Lett., 2005, 7, 1247-50. Cycloruthenated Primary and Secondary Amines as Efficient Catalyst Precursors for Asymmetric Transfer Hydrogenation.
75.H. Bernsmann, M. van den Berg, R. Hoen, A. J. Minnaard, G. Mehler, M. T. Reetz, J. G. de Vries, and B. L. Feringa, J. Org. Chem., 2005, 70, 943-951. PipPhos and MorfPhos: Privileged Monodentate Phosphoramidite Ligands for Rhodium-Catalyzed Asymmetric Hydrogenation.
74.M. D. K. Boele, P. C. J. kamer, M. Lutz, A. L. Spek, J. G. de Vries, P. W. N. M. van Leeuwen and G. P. F. van Strijdonck, Chem. Eur. J., 2004, 10, 6232-6246. Bulky monodentate phosphoramidites in palladium-catalyzed allylic alkylation reactions: Aspects of regioselectivity and enantioselectivity.
73.A. Duursma. J.-G. Boiteau, L. Lefort, J. A. F. Boogers, A. H. M. de Vries, J. G. de Vries, A. J. Minnaard and B. L. Feringa, J. Org. Chem. , 2004, 69, 8045-8052. Highly enantioselective conjugate additions of potassium organotrifluoroborates to enones by use of monodentate phosphoramidite ligands.
72.A. H. M. de Vries and J. G. de Vries, Adv. Synth. Catal., 2004, 346, 1812. Use of “homeopathic” ligand-free palladium as catalyst for aryl-aryl coupling reactions. A. Alimardanov, L. Schmieder-van de Vondervoort
71.X.-b. Jiang, M. van den Berg, A. J. Minnaard, B. L. Feringa and J. G. de Vries, Tetrahedron: Asymmetry, 2004, 15, 2223-2229. The application of monodentate secondary phosphine oxide ligands in rhodium- and iridium-catalyzed asymmetric hydrogenation.
70.M.T. Reetz and J.G. de Vries, Chem. Commun., 2004, 1559-1563. Ligand-free Heck reactions using low Pd-loading.
69.D. Ager, M. van den Berg, A. J. Minnaard, B. L. Feringa, A. H. M. de Vries, C. E. Willans, J. A.F. Boogers and  J. G. de Vries, in Methodologies in Asymmetric Catalysis. Ed. Sanjay V. Malhotra, ACS Symposium Series No. 880, Oxford University Press,  New York, NY, USA, 2004, 115-129. An Affordable Catalyst for the Production of Amino Acids.
68.D. Ager, J.G. de Vries, L. Lefort, A.H. M. de Vries, J.A.F. Boogers, Pharmachem, 2004, 3 (6), 38. Alleviating the problems of fitting a square peg in a round hole.
67.M. van den Berg, D. Peña, A. J. Minnaard, B. L. Feringa, L. Lefort, J. A. F. Boogers, A. H. M. de Vries and J. G. de Vries, Chimica Oggi, 200422 (5),  Supplement on Asymmetric Hydrogenation, 18-21. Instant Ligand Libraries of Monodentate Phosphoramidites. Asymmetric Hydrogenation made Easy.
66.S. Basra, J. G. de Vries, D. J. Hyett, G. Harrison, K. M. Heslop, A. G. Orpen, P. G. Pringle, K. von der Luehe, J. Chem. Soc. Dalton Trans., 2004, 1901-1904. Efficient asymmetric hydrogenation with rhodium complexes of C1-symmetric 2,5-dimethylphospholane-diphenylphosphines.
65.A. Duursma, L. Lefort, J. A. F. Boogers, A. H. M. de Vries, J. G. de Vries, A. J. Minnaard  and Ben L. Feringa, Org. Biomol. Chem., 2004, 2, 1682-1684. Synthesis and application in asymmetric C–C bond formation of solution phase ligand libraries of monodentate phosphoramidites.
64.L. Lefort, J. A. F. Boogers, A. H. M. de Vries and J. G. de Vries, Org. Lett., 2004, 6, 1733-1735. Instant Ligand Libraries. Parallel Synthesis of Monodentate Phosphoramidites and in Situ Screening in Asymmetric Hydrogenation.
63.R. Hoen, M. van den Berg, H. Bernsmann, A. J. Minnaard, J. G. de Vries and B. L. Feringa, Org. Lett., 2004, 6, 1433-1436. Catechol-Based Phosphoramidites: A New Class of Chiral Ligands for Rhodium-Catalyzed Asymmetric Hydrogenations.
62.X.-b. Jiang, A. J. Minnaard, B. L. Feringa, J. G. de Vries, J. Org. Chem., 2004, 69, 2327-2331. Platinum-Catalyzed Selective Hydration of Hindered Nitriles and Nitriles with Acid- or Base-Sensitive Groups.
61.C. E. Willans, J. M.C.A. Mulders, J. G. de Vries, A. H.M. de Vries J. Organomet. Chem., 2003, 687, 494-497. Ligand-free palladium catalysed Heck reaction of methyl 2-acetamido-acrylate and aryl bromides as key step in the synthesis of enantiopure substituted phenylalanines.
60.M.C. van Engelen, H.T. Teunissen, J.G. de Vries and C.J. Elsevier, J. Mol. Catal. A: Chem.,  2003, 206, 185-192. Suitable ligands for homogeneous ruthenium-catalyzed hydrogenolysis of esters.
59.A.H.M. de Vries, J.M.C.A. Mulders, J.H.M. Mommers, H.J.W. Henderickx and J.G. de Vries, Org. Lett., 2003, 5, 3285-8. Homeopathic ligand-free palladium as a catalyst in the Heck reaction. A comparison with a palladacycle.
58.J.G. de Vries, A.H.M. de Vries, J.A.F. Boogers, M. van den Berg, D. Peña, A.J. Minnaard, B.L. Feringa, Process Ingenuity. Pharmaceutical & Fine Chemicals. 2003, September issue, p2-8. Monodentate phosphoramidites. A breakthrough in asymmetric olefin hydrogenation for fine chemicals.
57.A.H.M. de Vries, J.A.F. Boogers, M. van den Berg, D. Peña, A.J. Minnaard, B.L. Feringa, J.G. de Vries. PharmaChem 2003, Sept, 33-36. Affordable asymmetric olefin hydrogenation using monodentate phosphoramidites.
56.X.-B. Jiang, A.J. Minnaard, B. Hessen, B.L. Feringa, A.L.L. Duchateau, J.G.O. Andrien, J.A.F. Boogers and J.G. de Vries, Org. Lett., 2003, 5, 1503-1506. Application of monodentate secondary phosphine oxides, a new class of chiral ligands, in Ir(I)-catalyzed asymmetric imine hydrogenation.
55.D. Peña , A. J. Minnaard , J. A. F. Boogers , A. H. M. de Vries, J. G. de Vries and B. L. Feringa Org. Biomol. Chem., 20031, 1087 – 1089. Improving conversion and enantioselectivity in hydrogenation by combining different monodentate phosphoramidites; a new combinatorial approach in asymmetric catalysis.
54.M.M.H. Lambers-Verstappen and J.G. de Vries, Adv. Synth. Catal. 2003, 345, 478-482. Rhodium-catalysed asymmetric hydroformylation of unsaturated nitriles.
53.J.G. de Vries and A.H.M. de Vries, Eur. J. Org. Chem., 2003, 799-811. The power of high-throughput experimentation in homogeneous catalysis research for fine chemicals.
52.D. Peña, A.J. Minnaard, A.H.M. de Vries, J.G. de Vries and B.L. Feringa, Org. Lett., 2003, 5, 475-478. Mono- versus bidentate ligands in asymmetric hydrogenation. A comparative rate study.
51.M. van den Berg, A.J. Minnaard, R.M. Haak, M. Leeman, E.P. Schudde, A. Meetsma, B.L. Feringa, A.H.M. de Vries, C.E.P. Maljaars, C.E. Willans, D.J. Hyett, J.A.F. Boogers, H.J.W. Henderickx, J.G. de Vries, Adv. Synth. Catal. 2003, 345, 308-322. Monodentate phosphoramidites. A breakthrough in rhodium catalysed asymmetric hydrogenation of olefins.
50.J.G. de Vries in Encyclopedia of Catalysis, Istvan T. Horvath, ed., John Wiley & Sons, New York, 2003, Vol 3, 295-347. Fine Chemical Synthesis. Homogeneous.
49.D. Peña, A.J. Minnaard, J.G. de Vries and B.L. Feringa, J. Am. Chem. Soc., 2002, 124, 14552-3. Highly enantioselective rhodium-catalyzed hydrogenation of β-dehydroamino acid derivatives using monodentate phosphoramidites
48.M. van den Berg, R.M. Haak, A.J. Minnaard, A.H.M. de Vries, J.G. de Vries and B.L. Feringa, Adv. Synth. Catal., 2002, 344, 1003-1007. Rhodium/MonoPhos-catalysed asymmetric hydrogenation of enamides.
47.A.H.M. de Vries, F.J. Parlevliet, L. Schmieder-van de Vondervoort, J.H.M. Mommers, H.J.W. Henderickx, M.A.N. Walet and J.G. de Vries, Adv. Synth. Catal., 2002, 344, 996-1002. A practical recycle of ligand-free palladium catalyst for Heck reactions.
46.M. Lambers, F.H. Beijer, J.M. Padron, I. Toth and J.G. de Vries, J. Org. Chem., 2002, 67, 5022-5024. Highly selective hydroformylation of the Cinchona alkaloids.
45.B. Baragaña, A. G. Blackburn, P. Breccia, A. P. Davis, J. de Mendoza, J. M. Padrón-Carrillo, P. Prados, J. Riedner, and J. G. de Vries, Chem. Eur. J. , 2002, 8, 2931-6. Enantioselective Transport by a Steroidal Guanidinium Receptor.
44.A. Jutand, S. Negri and J.G. de Vries, Eur. J. Inorg. Chem., 2002, 1711-1717. Rate and mechanism of the oxidative addition of benzoic anhydride to palladium(0) complexes in DMF.
43.C.E. Tucker and J.G. de Vries, Topics in Catalysis, 2002, 19, 111-118. Homogeneous catalysis for the production of fine chemicals. Palladium and nickel catalysed aromatic carbon-carbon bond formation.
42.M.D.K. Boele, G.P.F. van Strijdonck, A.H.M. de Vries, P.C.J. Kamer, J.G. de Vries and P.W.N.M. van Leeuwen, J. Am. Chem. Soc., 2002, 124, 1586-7. Selective Pd-catalyzed oxidative coupling of anilides with olefins through C-H bond activation at room temperature.
41.E.G. IJpeij, F.H. Beijer, H.J. Arts, C. Newton, J.G. de Vries and G.J. Gruter, J. Org. Chem., 2002, 67, 169-176. A Suzuki coupling based route tot 2,2’-bis(2-indenyl)biphenyl derivatives.
40.R. Chen, C. Qian, J.G. de Vries and L. Wang,  Chin. J. Chem. 2001,  19, 1225-1231. Asymmetric catalytic epoxidation of enones by chiral binaphthol-derived lanthanum catalyst.
39.R. Chen, C. Qian and J.G. de Vries, Tetrahedron., 2001,  57, 9837-9842. Highly efficient enantioselective epoxidation of α,β-enones catalyzed by cheap chiral lanthanum and gadolinium alkoxides
38.R. Chen, C. Qian and J.G. de Vries, Tetrahedron Lett., 2001, 42, 6919-6921. Asymmetric epoxidation of α,β-unsaturated ketones catalyzed by chiral ytterbium complexes.
37.J.G. de Vries, A.H. M. de Vries, C.E. Tucker and J.A. Miller, Innovations Pharm. Tech. , 2001, 1 (8), 125-130. Palladium catalysis in the production of pharmaceuticals.
36.J.G. de Vries, Can.J. Chem., 2001, 79, 1086-1092. The Heck reaction in the production of fine chemicals.
35.A.J. Minnaard, M. van den Berg, E.P. Schudde, J. van Esch, A.H.M. de Vries, J.G. de Vries and B.L. Feringa, Chimica Oggi / Chem. Today 2001, 19 (3/4), 12-13. Yes! Asymmetric hydrogenation with cheap ligands!
34.M.S. Stephan and J.G. de Vries in Chemical Industries 82, Catalysis of Organic Reactions, M.E. Ford, Ed., Marcel Dekker, Inc., New York, 2000, p379-390. Homogeneous Catalysis for Fine Chemicals: The Heck Reaction as Clean Alternative for Friedel-Crafts Chemistry.
33.M. van den Berg, A.J. Minnaard, E.P. Schudde, J. van Esch, A.H.M. de Vries, J.G. de Vries and B.L. Feringa, J. Am. Chem.Soc., 2000, 122, 11539-40. Highly enantioselective rhodium-catalyzed hydrogenation with monodentate ligands.
32.M. van den Heuvel, A. Abbadi and J.G. de Vries, Tetrahedron Lett., 2000, 2467-2470. Platinum catalysed hydrolytic amidation of unactivated nitriles. C.J. Cobley.
31.D.D. Ellis, G. Harrisson, A.G. Orpen, H. Phetmung, P.G. Pringle, J.G. de Vries and H. Oevering, J. Chem.Soc.., Dalton Trans., 2000, 671-675. Platinum(II), palladium(II) and rhodium(I) complexes of o-, m-, and p- Ph2PC6H4PO(OEt)2. PtCl2-SnCl2 Hydroformylation catalysts modified with phosphonated triarylphosphines.
30.J.G. de Vries, B.J.R. Scholtens, I. Maes, M. Grätzel, S. Winkel,. S. Burnside, M. Wolf, A. Hinsch, J.M. Kroon, M. Ahlse, F. Tjerneld, G. Ferrero, E. Bruno, A. Hagfeldt, C. Bradbury, P. Carlsson, H. Pettersson, C.M. Verspeek-Rip and I.C. Enninga, Solar Energy Materials & Solar Cells, 2000, 60, 43-49. Negative Ames test of cis-di(thiocyanato)-N,N’-bis(4,4’-dicarboxy-2,2’-bipyridine)Ru(II), the sensitizer dye of the nanocrystalline TiO2 solar cell.
29.D.G.I. Petra, P.C.J. Kamer, P.W.N.M. van Leeuwen, K. Goubitz, A.M. van Loon, J.G. de Vries and H.E. Schoemaker, Eur. J. Inorg. Chem., 1999, 2235-2341. Amino alcohol coordination in ruthenium(II)-catalysed asymmetric transfer hydrogenation of ketones.
28.G.P.F. van Strijdonck, M.D.K. Boele, P.C.J. Kamer, J.G. de Vries and P.W.N.M. van Leeuwen, Eur. J. Inorg. Chem. 1999, 1073-1076. Fast palladium catalyzed arylation of alkenes using bulky monodentate phoshorus ligands.
27.J. G. de Vries, G. Roelfes and R. Green, Tetrahedron Lett., 1998, 39, 8329. Ruthenium catalysed redox transformation of cinnamaldehyde to 3-phenylpropionic acid and methyl ester.
26.J. G. de Vries and M. S. Stephan, Spec. Chem., 1998, 18 (5), 202. Olefin arylations without waste-the Heck reaction.
25.M. S. Stephan, A. J. J.M. Teunissen, G. K. M. Verzijl and J. G. de Vries, Angew. Chem. Int. Ed. Engl., 1998, 37, 662. Heck reactions without salt formation: Aromatic carboxylic anhydrides as arylating agents.
24.I. Toth, C.J. Elsevier, J.G. de Vries, J. Bakos, W.J.J.    Smeets and A. L. Spek, J. Organomet. Chem., 1997, 540, 15. Synthesis of Pt compounds containing chiral (2S, 4S)-pentane-2,4-diyl-bis(5H-dibenzo[b]phosphindole) as ligand and their use in asymmetric hydroformylation of styrene derivatives.
23.J.G. de Vries, R.P. de Boer, M. Hogeweg and E.E.C.G. Gielens, J. Org. Chem., 1996, 61, 1842. Influence of degree of sulfonation of BDPP upon enantioselectivity in rhodium-     BDPP catalyzed hydrogenation reactions in a two phase system. C. Lensink, E. Rijnberg and J.G. de Vries, J. Mol. Catal. A: Chem., 1997, 116, 199.23. Preparation of d,l- Phenylalanine by amidocarbonylation of benzyl chloride.
22.J.G.H. Willems, J.G. de Vries, R.J.M. Nolte and B.       Zwanenburg,  Tetrahedron Letters, 1995, 36, 3917. Asymmetric synthesis of amines via chiral base catalysed [1,3]-proton shift reaction of imines.
21.J. G. de Vries, Encyclopedia for Reagents in Organic Synthesis, L.A. Paquette, Ed., Wiley&Sons, 1995; Vol 3, p 1890. Dihydroxyphenylborane.
20.C. Lensink and J.G. de Vries, Tetrahedron Asymme­try, 1993, 4, 215. Diastereoselective hydrogenation and kinetic resolution of imines using rhodium/diphoshosphine catalyzed hydrogenation.
19.D. Callant, D. Stanssens and J. G. de Vries, Tetrahedron     Asymmetry, 1993, 4, 185. (S)-3,3-Dimethyl-1,2,4-butanetriol as ligand for titanium catalysed asymmetric silylcyanation.
18.D. Cal­lant, B. Coussens, T. van der Maten, J. G. de Vries and N. K. de Vries, Tetrahedron Asymmetry, 1992, 3, 401. NMR measurements and semiempirical calculations in a first approach to elucidate the mechanism of enantioselective cyano­hydrin formation catalysed by cyclo-(S)-Phe-(S)-His.
17.H. Moorlag, J. G. de Vries, B.Kaptein, H. E. Schoemaker, J. Kamp­huis and R. M. Kellogg., Recl. Trav. Chim.Pays-Bas, 1992, 111, 129. Palladium catalyzed allylation of α-hydroxy acids.
16.C. Lensink and J. G. de Vries, Tetrahedron Asymme­try, 1992, 3, 235. Improving enantioselectivity by using a monosulfonated diphosphine ligand for homogeneous imine hydrogenation.
15.An iodinatable photoaffinity probe based on the structure of Kallidin, Adv. Exp. Med. Biol., 1989, 247A(Kinins 5, Pt. A), 409.
14.J.G. de Vries, E. Phillips, C.R. Snell, P.H. Snell and M. Webb, J. Neurochem., 1989, 52, 1508. Construction of a physiologically active photoaffinity probe based on the structure of Bradykinin: labeling of angio­tensin converting enzyme but not candidate Bradykinin recep­tors on NG108-15 cells.
13.J.G. de Vries and S.A. Hubbard, J. Chem. Soc. Chem. Commun., 1988, 1172. Conversion of benzoin into 9,10-phenanthrenequinone by photocyclisation.
12.M. Webb, J.G. de Vries, C. Snell and E. Phillips, Protides Biol. Fluids, 1987, 35, 419. Identification of Bradykinin receptors on NG108-15 hybrid celles.
11.C.R. Snell, J.G. de Vries, E. Phillips and M. Webb, Biochem. Soc. Trans. 1987, 15, 890. Photoaffinity labeling of Bradykinin receptors on NG108-15 hybrid cells.
10.J.G. de Vries and G. Sigmund , Tetrahedron Lett, 1985, 26, 2765. Synthesis of 3-aminoalkyl substituted carbapenems via a phosphorane intermediate.
9.J.G. de Vries, G. Sigmund and G. Vorisek, Heterocy­cles, 1985, 23, 1915. Synthesis of carbapenems with a RXCH2-substituent in the 3-position.
8.J.G. de Vries, G. Hauser and G. Sigmund, Heterocycles, 1985, 23, 1081. Facile retro Dieckmann reactions of 3-oxocarbapenam es­ters.
7.A.G. Talma, P. Jouin, J.G. de Vries, C.B. Troostwijk, G.H. Werumeus Buning, J.K. Waninge, J. Visscher and R.M. Kellogg, J. Am. Chem. Soc., 1985, 107, 3981. Reductions of activated carbonyl compounds with chiral, bridged 1,4-dihydropyridi­nes. An investigation of scope and structural effects.
6.J.B. Hen­drickson and J.G. de Vries, J. Org. Chem., 1985, 50, 1688. Total synthesis of the novel coenzyme Methoxatin.
5.J.G. de Vries, G. Hauser and G. Sigmund, Tetrahedron Lett., 1984, 25, 5989. Synthesis of carbapenems with carbon substituents at C-3 using a Wittig approach.
4.J.B. Hen­drick­son and J.G. de       Vries, J. Org. Chem., 1982, 47, 1148. A convergent total synthesis of Methoxatin.
3.J.G. de Vries and R.M. Kellog, J. Org. Chem. 1980, 45, 4126. Reductions of aldehydes and ketones by sodium dithionite.
2.J.G. de Vries and R.M. Kellogg, J. Am. Chem. Soc., 1979, 101, 2759. Asymmetric reductions with a chiral 1,4-dihydropyridine crown ether.
1.J.G. de Vries, T.J. van Bergen and R.M. Kellogg, Synthe­sis, 1977, 246. Sodium dithionite as a reductant for aldehydes and keto­nes.
38.A. Marckwordt, H. Amani, N. Kalevaru, S. Wohlrab, P. Kamer, J. de Vries, Verfahren zur Herstellung von endständig ungesättigtem Alkencarbonsäureester aus Lactonen, DE 102018114441.5, (15.06.2018)
37.M. Beller, W. Bonrath, J. de Vries, Y. Fan, S. Hübner, L. Lefort, J. Medlock, P. Puylaert, R. van Heck, M. Kurt, (DSM Nutritional Products ltd.), Selective Reduction of Esters to Alcohols, EP 1619509.5, WO2017194663 (13.05.2016).
36.M. Beller, W. Bonrath, J. de Vries, Y. Fan, S. Hübner, L. Lefort, J. Medlock, P. Puylaert, R. van Heck, M. Kurt, (DSM Nutritional Products ltd.), Selective Reduction of Aldehydes and Ketones, EP 16169508.5, WO2017194662 (13.05.2016).
35.Process for the preparation of 5-formylvaleric acid and adipic acid. R. F. M. J. Parton, M. C. C. Janssen, B. Engendahl, J. G. de Vries, WO2014/111446, to DSM IP Assets B.V.
34.Process for the production of furfural and levuilinic acid from lignocellulosic biomass. J. G. de Vries, J. A. Kroon, R. F. M. J. Parton, P. L. Woestenborghs, A. De Rijke, WO2014/009521, to DSM IP Assets B.V.
33.Selective oxidation of carbohydrates. A. J. Minnaard, M. Jäger, A. L. N. R. Gottumukkala, J. G. de Vries, A. A. Bastian, A. Hermann, WO 2013/191549, to Rijksuniversiteit Groningen.
32.Process to produce alkanoic acid esters in a carbonylation process using Lewis acids as acid promotor. M. C. C. Janssen, J. G. de Vries,  WO2013/107904, to DSM IP Assets B. V.
31.Process for the separation of a dissolved catalyst system from an alkoxycarbonylation reaction mixture. J. G. de Vries, M. C. C. Janssen, R. F. M. J. Parton, H. D. Hoving, WO2013/107902, to DSM IP Assets B. V.
30.Process for the isomerisation of substituted alkenes. N. Sereinig, M. C. C. Janssen, J. G. de Vries, WO 2013/013990, to DSM IP Assets B. V.
29.Process for the preparation of alkanoic acid esters in a carbonylation process using palladium bidentate biphosphate ligands. J. G. de Vries, N. Sereinig, E. W. M. van de Vondervoort, M. C. C. Janssen, WO 2012/131027, to DSM IP Assets B. V.
28.Process for the preparation of 3-methylene-γ-valerolactone. S. M. A. de Wildeman, J. G. de Vries, J. A. F. Boogers, WO 2012/116997, to DSM IP Assets B. V.
27.Preparation of caprolactone, caprolactam, 2,5-tetrahydrofuran-dimethanol, 1,6-hexanediol or 1,2,6-hexanetriol from 5-hydroxymethyl-2-furfuraldehyde. J. G. de Vries, Teddy, P. H. Phua, I. V. Melián Cabrera, H. J. Heeres, WO 2011/149339, to Netherlands Organisation for Scientific Research (Advanced Chemical Technologies for Sustainability).
26.Novel N-substituted beta-amino acid esters. G. F. Busscher, J. G. de Vries, L. Lefort, WO 2010/006954, to DSM IP Assets B. V.
25.Use of dissolved iron nanoparticles as catalyst in addition reactions. J. G. de Vries, L. Lefort, P. H. Phu, WO 2009/150173, to DSM IP Assets B. V.
24.Convergent synthesis of renin inhibitors and intermediates useful therein. B. de Lange, A. M. C. F. Castelijns, J. G. de VRies, A. H. M. De Vries,  J. A. F. Boogers, Q. B. Broxterman, WO 2009/ 080773, to DSM IP Assets B. V.
23.Boron-catalyzed peptide synthesis. P. J. L. M. Quaedflieg, T. Nuijens, J. G. de Vries, H. A. Van Kalkeren, EP2107067, 2009, to DSM IP Assets B.V.
22.Asymmetric hydrogenation of prochiral compounds, J. G. de VRies, B. Stegink, WO 2008/077610, to DSM IP Assets B. V.
21.Process for production of styrene derivative. S.-I. Kuwabe, H. Masaoka, K.-H. Giselbrecht, J. Hiebl, K. Reiter,  W. Skranc, A. H. M. de Vries, J. G. de Vries, WO 2008/010578,  to Ono Pharmaceutical Co. Ltd.
20.Continuous chemical processes in centrifugal contact separators. J. G. de Vries, G. J. Kwant, H. J. Heeres, WO 2007/031332, to DSM IP Assets B.V.
19.Process for the preparation of enantiomerically enriched indoline-2-carboxylic acids via cyclization of phenylalanine derivatives. A. H. M. de Vries, J. G. de Vries, F. B. J. Van Assema, B. De Lange, D. Mink, D. J. Hyett, P. J. D. Maas, WO 2006/069799 to DSM IP Assets B.V.
18.Process for transition metal-catalyzed asymmetric hydrogenation of acrylic acid derivatives, and novel catalyst system for asymmetyric transition metal catalysis. J. A. F. Boogers, U. Felfer, M. Kotthaus, A. H. M. de Vries, J. G. de Vries, L. Lefort, G. Steinbauer, WO 2006/069617, to DSM Fine Chemicals Austria Nfg, G. m.b.H & Co. K.-G.
17.Continuous process for the enantioselective enrichment and separation of enantiomers using centrifugal separation. J. G. de Vries, G. J. Kwant, A. J. Hallett, EP 1676614, 2006, to DSM IP Assets B.V.
16.Process for the preparation of enantiomerically enriched indoline-2-carboxylates via cyclization of substituted phenylalanines.J. G. de Vries, B. de Lange, A. H. M. de Vries, D. Mink, F. B. J. van Assema, P. J. D. Maas, D. J. Hyett, EP1676838, 2006, to DSM IP Assets B.V.
15.Chiral compound suitable as a catalyst for asymmetric transfer hydrogenation. J. G. de Vries, G. K. M. Verzijl, A. H. M. De Vries, V. Ritleng, A. M. J. Voelklin, WO 2006/050988, to DSM IP Assets B.V.
14.Process for the preparation of (hetero)arylamines by arylation of amines with aryl bromides using copper catalysts and oxygen-containing ligands. M. M. H. Lambers, B. de Lange, A. H. M. de Vries, J. G. de Vries, N. Sereinig, WO 2006/009431, to DSM IPO Assets B.V.
13.Process for a homogeneously catalyzed C-C coupling reaction.  A.H.M. de Vries and J.G. de Vries, WO 02/057199, to DSM n.v.
12.Catalyst for asymmetric (transfer) hydrogenation. M. van den Berg, A. J. Minnaard, B. L. Feringa, J.G. de Vries, WO 02/04466, to DSM n.v.
11.Process for regenerating palladium catalysts. F.J. Parlevliet, A.H.M. de Vries and J.G. de Vries, WO 02/00340, to DSM n.v.
10.Process for the preparation of enantiomerically enriched esters and alcohols. G. K. M. Verzijl, J. G. de Vries, Q. B. Broxterman, WO 01/90396, to DSM n.v.
9.Catalyst for asymmetric transfer hydrogenation. D.G. I. Petra, P.C.J. Kamer, P.W.N.M. van Leeuwen, J.G. de Vries, H.E. Schoemaker, WO 01/023088, to DSM n.v.
8.Process and arylation catalysts for preparing a (hetero)arylalkene from an alkene and a (hetero)arylcarboxylic anhydride, J. G. de Vries, M. S. Stephan, WO 98/049128, to DSM n.v.
7.Process for the preparation of heterocyclic o-dicarboxylic acids, G.H. Suverkropp, P.L. Alsters, C.S. Snijder and J.G. de Vries, EP 847993, 1998, to DSM n.v.
6.Cyclopentadiene compounds substituted by chiral groups, metal complexes thereof, and alpha-olefin polymerisation catalysts containing the same, G. J. M. Gruter, J. A. M. van Beek and J. G. de Vries, WO 97/042151, to DSM n.v.
5.Preparation of cyclic N-alkenyloxyimides and the corresponding cyclic N-alkoxyimides and O-alkoxyamines. D. M. C. Callant, A. M. C. Castelijns, J. G. de Vries, WO 95/025090, to DSM n.v.
4.Bidentate phosphine ligand. P. C. J. Kamer, M. Kranenburg, P. W. N. M. van Leeuwen, J. G. de Vries, WO 95/030680 to DSM n.v.
3.Process for the preparation of 5-formylvaleric acid and 5-formylvalerate ester. C. B. Hansen, J. G. de Vries, WO 95/018089, to DSM n.v.
2.Process for the preparation of a linear aldehyde organic compound. A. J. J. M. Teunissen, J. G. de Vries, O. J. Gelling, C. Lensink, WO 94/026688, to DSM n.v.
1.Indenyl compounds substituted at the two-position and their use as catalysts for olefin polymerisation. J. A. M. van Beek, J. G. de Vries, H. J. Arts, R. Persad, G. H. J. van Doremaele, WO 94/011406, to DSM n.v.