Nicolas Sevrain
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Interests
Nicolas Sevrain has a total of 4 co-authors. Here are the top co-authors by number of shared publications:
- David Virieux
ICGM, Univ Montpellier, ENSCM, CNRS, 34090 Montpellier, France
1 shared publication - Jean-Luc Pirat
ICGM, Univ Montpellier, ENSCM, CNRS, 34090 Montpellier, France
1 shared publication - Jean-Noël Volle
ICGM, Univ Montpellier, CNRS, ENSCM, 34293 Montpellier, France
1 shared publication - Tahar Ayad
ICGM, Univ Montpellier, ENSCM, CNRS, 34090 Montpellier, France
1 shared publication
Latest Publications
- 17 May 2018
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2018 (19) , 2267-2272
Chiral Bisdiphenylphosphine Dioxides Bearing a Bis(triazolyl) Backbone as Promising Lewis Bases for Asymmetric Organocatalysis
Two chiral C2‐symmetric diphenylphosphine dioxides bearing an original bis(triazolyl) backbone were prepared starting from inexpensive and readily available precursors. The key step involves the simultaneous formation of five bonds in one chemical step with 100 % atom efficiency through a copper‐catalyzed tandem [3+2] cycloaddition/dimerization reaction. Interestingly, these chiral inducers exhibited good to excellent catalytic activities as chiral Lewis base organocatalysts to promote useful stereoselective reactions.
- 17 May 2018
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2018 (19) , 2267-2272
Chiral Bisdiphenylphosphine Dioxides Bearing a Bis(triazolyl) Backbone as Promising Lewis Bases for Asymmetric Organocatalysis
Two chiral C2‐symmetric diphenylphosphine dioxides bearing an original bis(triazolyl) backbone were prepared starting from inexpensive and readily available precursors. The key step involves the simultaneous formation of five bonds in one chemical step with 100 % atom efficiency through a copper‐catalyzed tandem [3+2] cycloaddition/dimerization reaction. Interestingly, these chiral inducers exhibited good to excellent catalytic activities as chiral Lewis base organocatalysts to promote useful stereoselective reactions.