Enantioselective rearrangement of exo-norbornene oxide to nortricyclanol
The enantioselective α-deprotonation-rearrangement of exo-norbornene oxide 1 to (-)-nortricyclanol 2 in up to 52% ee using a nonracemic lithium amide, or an organolithium in the presence of (-)-sparteine, is described.
Glavni autori: | Hodgson, D, Wisedale, R |
---|---|
Format: | Journal article |
Jezik: | English |
Izdano: |
1996
|
Slični predmeti
-
Titanium-porous catalysts for the oxidation of norbornene to norbornene oxide /
od: Teow, Bee Khuan, 1986-, i dr.
Izdano: (2009) -
An enantioselective epoxide rearrangement - Claisen rearrangement approach to prostaglandins and (+)-iridomyrmecin
od: Hodgson, D, i dr.
Izdano: (1997) -
NMR Spectroscopic Studies on (exo, endo) C-2 Monosubstituted Norbornene Derivatives
od: Zi-hao WANG, i dr.
Izdano: (2021-09-01) -
Enantioselective alpha-deprotonation-rearrangement of meso-epoxides
od: Hodgson, D, i dr.
Izdano: (1996) -
Synthesis of AI-MCM-41/ZSM-5 composite for oxidation of norbornene to norbornene oxide /
od: Faridah Abu Bakar, 1985-, i dr.
Izdano: (2010)