Abstract
Diastereoselective Michael additions of 2-hydrogeno-2-oxo-1,4,2-oxazaphosphinanes to olefins were described. Phosphinopeptide compounds were obtained in very good yield (up to 90%) and diasteromeric excesses ranging from 26 to 78%.
- Title
- Diastereoselective Michael addition of 2H-2-oxo-1,4,2-oxaza phosphinanes to olefins
- Creators - without role
- Jérôme Monbrun - Université de Montpellier, Institut Charles Gerhardt Montpellier - ICGMBénédicte Dayde - Université de Montpellier, Institut Charles Gerhardt Montpellier - ICGMHenri-Jean Cristau - Université de Montpellier, Institut Charles Gerhardt Montpellier - ICGMJean-Noël Null Volle - Université de Montpellier, Institut Charles Gerhardt Montpellier - ICGMDavid Null Virieux - Université de Montpellier, Institut Charles Gerhardt Montpellier - ICGMJean-Luc Pirat - Université de Montpellier, Institut Charles Gerhardt Montpellier - ICGM
- Publication Details
- Tetrahedron, Vol.67, pp.540-545
- Identifiers
- 9942123409311
- Academic Unit
- Institut Charles Gerhardt Montpellier - ICGM
- Language
- English
- Resource Type
- Journal article
- Local Fields
- hal-00633566