D-Index & Metrics Best Publications

Roland Furstoss

Centre national de la recherche scientifique, CNRS
France

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name Citations Publications World Ranking National Ranking

Chemistry D-index 51 Citations 6,109 145 World Ranking 10458 National Ranking 402

Overview

What is he best known for?

The fields of study Roland Furstoss is best known for:

Enzyme
Catalysis
Epoxide

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.

His most cited work include:

Enhancing the Enantioselectivity of an Epoxide Hydrolase by Directed Evolution (146 citations)
SYNTHESIS OF ENANTIOPURE EPOXIDES THROUGH BIOCATALYTIC APPROACHES (144 citations)

What are the main themes of his work throughout his whole career to date

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.

Roland Furstoss most often published in these fields:

Organic chemistry (90.00%)
Catalysis (90.00%)
Enantioselective synthesis (60.00%)

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Synthetic applications of epoxide hydrolases

Alain Archelas;Roland Furstoss.
Current Opinion in Chemical Biology (2001)

301 Citations

Towards large-scale synthetic applications of Baeyer-Villiger monooxygenases

Veronique Alphand;Giacomo Carrea;Roland Wohlgemuth;Roland Furstoss.
Trends in Biotechnology (2003)

233 Citations

Enhancing the enantioselectivity of an epoxide hydrolase by directed evolution.

Manfred T. Reetz;Claudia Torre;Andreas Eipper;Renate Lohmer.
Organic Letters (2004)

192 Citations

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)

183 Citations

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)

171 Citations

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)

155 Citations

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)

144 Citations

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.
Tetrahedron (1996)

137 Citations

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)

133 Citations

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.
Tetrahedron-asymmetry (2004)

126 Citations

If you think any of the details on this page are incorrect, let us know.