Alain Archelas - Concepedia

Author

Alain Archelas

Centre National de la Recherche Scientifique

Also Known As

A Archelas, A. ARCHELAS, A. Archelas, Alain ARCHELAS, Alain Archelas, Archelas, A., Archelas, Alain

121

Publications

Citations

H-Index

Concepts

All Affiliations

Centre National de la Recherche Scientifique Laboratoire de Chimie Organique Institut de Neurobiologie de la Méditerranée Czech Academy of Sciences Czech Academy of Sciences, Institute of Microbiology

About

Alain Archelas is an author at Centre National de la Recherche Scientifique specializing in biochemistry, natural sciences, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biochemistry	29	52	2.3K
2	Natural Sciences	26	47	2.1K
3	Engineering	25	38	1.8K
4	Medicine	12	12	501
5	Biology	2	2	33

Alain Archelas

Publications

3.3K

Citations

H-Index

Page 1

	Year	Citations
Enhancing the Enantioselectivity of an Epoxide Hydrolase by Directed Evolution Manfred T. Reetz, Claudia Torre, Andreas Eipper, Organic Letters	2003	156
Directed Evolution of an Enantioselective Epoxide Hydrolase: Uncovering the Source of Enantioselectivity at Each Evolutionary Stage Manfred T. Reetz, Marco Bocola, Li-Wen Wang, Journal of the American Chemical Society BiosynthesisEngineeringBiochemistryNatural SciencesBiocatalysis	2009	152
Microbiological transformations. 28. Enantiocomplementary epoxide hydrolyses as a preparative access to both enantiomers of styrene oxide S. PEDRAGOSA‐MOREAU, Alain Archelas, Roland Furstoss The Journal of Organic Chemistry Bioorganic ChemistryEngineeringChemical AnalysisAltmetric Attention ScoreOrganic Chemistry	1993	133
Microbial Transformations 16. One-step synthesis of a pivotal prostaglandin chiral synthon via a highly enantioselective microbiological Baeyer-Villiger type reaction Véronique Alphand, Alain Archelas, Roland Furstoss Tetrahedron Letters EngineeringBiotransformationDiversity-oriented SynthesisSynthetic BiologyOne-step Synthesis	1989	120
Microbiological Transformations. 33. Fungal Epoxide Hydrolases Applied to the Synthesis of Enantiopure <i>Para</i>-Substituted Styrene Oxides. A Mechanistic Approach S. PEDRAGOSA‐MOREAU, Christophe Morisseau, J. Zylber, The Journal of Organic Chemistry	1996	114
Microbiological transformation 32: Use of epoxide hydrolase mediated biohydrolysis as a way to enantiopure epoxides and vicinal diols: Application to substituted styrene oxide derivatives S. PEDRAGOSA‐MOREAU, Alain Archelas, Roland Furstoss Tetrahedron BiotransformationBiochemistryEpoxide HydrolaseNatural SciencesBiocatalysis	1996	105
Enzymatic transformations. Part 58: Enantioconvergent biohydrolysis of styrene oxide derivatives catalysed by the Solanum tuberosum epoxide hydrolase Marı́a I. Monterde, Murielle Lombard, Alain Archelas, Tetrahedron Asymmetry EngineeringBiotransformationBiochemistryNatural SciencesBiocatalysis	2004	102
Microbiological transformations. Part 45: A green chemistry preparative scale synthesis of enantiopure building blocks of Eliprodil: elaboration of a high substrate concentration epoxide hydrolase-catalyzed hydrolytic kinetic resolution process Kelath Murali Manoj, Alain Archelas, J. Baratti, Tetrahedron EngineeringBiotransformationBiochemistryMicrobiological TransformationsNatural Sciences	2001	95
Cloning and molecular characterization of a soluble epoxide hydrolase from Aspergillus niger that is related to mammalian microsomal epoxide hydrolase Michael Arand, Heike HEMMER, Heike Dürk, Biochemical Journal	1999	94
Microbiological transformations. 27. The first examples for preparative-scale enantioselective or diastereoselective epoxide hydrolyses using microorganisms. An unequivocal access to all four bisabolol stereoisomers X. J. Chen, Alain Archelas, Roland Furstoss The Journal of Organic Chemistry Bioorganic ChemistryBisabolol StereoisomersAltmetric Attention ScoreOrganic ChemistryChemistry	1993	92

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