a public good project by the
Synthesis
Company
of California

© 2026

Alain Archelas | doi.page

0 works0 citations0 h-index

Alain Archelas

Aix-Marseille Université(FR)Institut des Sciences Moléculaires de Marseille(FR)

Publications by Year

Research Areas

Enzyme Catalysis and Immobilization, Microbial Metabolic Engineering and Bioproduction, Steroid Chemistry and Biochemistry, Pharmacogenetics and Drug Metabolism, Chemical synthesis and alkaloids

Most-Cited Works

→ Synthetic applications of epoxide hydrolases(2001)226 cited
→ Enhancing the Enantioselectivity of an Epoxide Hydrolase by Directed Evolution(2003)156 cited
→ SYNTHESIS OF ENANTIOPURE EPOXIDES THROUGH BIOCATALYTIC APPROACHES(1997)153 cited
→ Directed Evolution of an Enantioselective Epoxide Hydrolase: Uncovering the Source of Enantioselectivity at Each Evolutionary Stage(2009)152 cited
→ Microbiological transformations. 28. Enantiocomplementary epoxide hydrolyses as a preparative access to both enantiomers of styrene oxide(1993)133 cited
→ Microbial Transformations 16. One-step synthesis of a pivotal prostaglandin chiral synthon via a highly enantioselective microbiological Baeyer-Villiger type reaction(1989)120 cited

→ Microbiological Transformations. 33. Fungal Epoxide Hydrolases Applied to the Synthesis of Enantiopure Para-Substituted Styrene Oxides. A Mechanistic Approach(1996)

114 cited

→ Microbiological transformation 32: Use of epoxide hydrolase mediated biohydrolysis as a way to enantiopure epoxides and vicinal diols: Application to substituted styrene oxide derivatives(1996)105 cited

→ Enzymatic transformations. Part 58: Enantioconvergent biohydrolysis of styrene oxide derivatives catalysed by the Solanum tuberosum epoxide hydrolase(2004)102 cited

→ 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(2001)95 cited