The Enantioselective synthesis portion of his research involves studies in Enantiopure drug and Kinetic resolution. Roland Furstoss performs multidisciplinary studies into Enantiopure drug and Enantioselective synthesis in his work. Roland Furstoss connects Combinatorial chemistry with Organic chemistry in his research. In his study, Roland Furstoss carries out multidisciplinary Organic chemistry and Combinatorial chemistry research. Borrowing concepts from Epoxide, Roland Furstoss weaves in ideas under Catalysis. He undertakes interdisciplinary study in the fields of Epoxide and Epoxide hydrolase through his works. His Biocatalysis study frequently draws parallels with other fields, such as Reaction mechanism. His research on Reaction mechanism frequently connects to adjacent areas such as Biocatalysis. His work on Selectivity is being expanded to include thematically relevant topics such as Catalysis.
Many of his studies on Ecology involve topics that are commonly interrelated, such as Substrate (aquarium) and Environmentally friendly. As part of his studies on Substrate (aquarium), Roland Furstoss frequently links adjacent subjects like Ecology. Roland Furstoss performs integrative Organic chemistry and Combinatorial chemistry research in his work. His multidisciplinary approach integrates Combinatorial chemistry and Organic chemistry in his work. He integrates many fields, such as Catalysis and Enantiomeric excess, in his works. In his work, Roland Furstoss performs multidisciplinary research in Enantiomeric excess and Enantioselective synthesis. His work on Dihydroxylation expands to the thematically related Enantioselective synthesis. Borrowing concepts from Biotransformation, Roland Furstoss weaves in ideas under Enzyme. Roland Furstoss performs multidisciplinary study in Enantiopure drug and Kinetic resolution in his work.
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Synthetic applications of epoxide hydrolases
Alain Archelas;Roland Furstoss.
Current Opinion in Chemical Biology (2001)
Towards large-scale synthetic applications of Baeyer-Villiger monooxygenases
Veronique Alphand;Giacomo Carrea;Roland Wohlgemuth;Roland Furstoss.
Trends in Biotechnology (2003)
Enhancing the enantioselectivity of an epoxide hydrolase by directed evolution.
Manfred T. Reetz;Claudia Torre;Andreas Eipper;Renate Lohmer.
Organic Letters (2004)
Microbiological transformations. 22. Microbiologically mediated Baeyer-Villiger reactions: a unique route to several bicyclic .gamma.-lactones in high enantiomeric purity
Veronique Alphand;Roland Furstoss.
Journal of Organic Chemistry (1992)
Microbiological transformations. 28. Enantiocomplementary epoxide hydrolyses as a preparative access to both enantiomers of styrene oxide
S. Pedragosa-Moreau;A. Archelas;R. Furstoss.
Journal of Organic Chemistry (1993)
Microbiological Transformations. 33. Fungal Epoxide Hydrolases Applied to the Synthesis of Enantiopure Para-Substituted Styrene Oxides. A Mechanistic Approach.
S. Pedragosa-Moreau;C. Morisseau;J. Zylber;A. Archelas.
Journal of Organic Chemistry (1996)
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 (1989)
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;A Archelas;R Furstoss.
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;Jacques Baratti.
Biochemical Journal (1999)
Enzymatic transformations. Part 58: Enantioconvergent biohydrolysis of styrene oxide derivatives catalysed by the Solanum tuberosum epoxide hydrolase
Maria I. Monterde;Murielle Lombard;Alain Archelas;Annette Cronin.
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