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.
Κύριοι συγγραφείς: | Hodgson, D, Wisedale, R |
---|---|
Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
1996
|
Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
-
Titanium-porous catalysts for the oxidation of norbornene to norbornene oxide /
ανά: Teow, Bee Khuan, 1986-, κ.ά.
Έκδοση: (2009) -
An enantioselective epoxide rearrangement - Claisen rearrangement approach to prostaglandins and (+)-iridomyrmecin
ανά: Hodgson, D, κ.ά.
Έκδοση: (1997) -
NMR Spectroscopic Studies on (exo, endo) C-2 Monosubstituted Norbornene Derivatives
ανά: Zi-hao WANG, κ.ά.
Έκδοση: (2021-09-01) -
Enantioselective alpha-deprotonation-rearrangement of meso-epoxides
ανά: Hodgson, D, κ.ά.
Έκδοση: (1996) -
Synthesis of AI-MCM-41/ZSM-5 composite for oxidation of norbornene to norbornene oxide /
ανά: Faridah Abu Bakar, 1985-, κ.ά.
Έκδοση: (2010)