A new and enantioselective indolizidine synthesis by meso-epoxide alpha-deprotonation-transannular N-C insertion
Enantioselective α-deprotonation-rearrangement of N-Boc hexahydroazonine oxide 10 using organolithiums in the presence of (-)-sparteine 3 gives the ester 12 in up to 89% ee.
Main Authors: | Hodgson, D, Robinson, L |
---|---|
Format: | Journal article |
Language: | English |
Published: |
1999
|
Similar Items
-
Enantioselective alpha-deprotonation-rearrangement of meso-epoxides
by: Hodgson, D, et al.
Published: (1996) -
Synthesis of (-)-xialenon A by enantioselective alpha-deprotonation-rearrangement of a meso-epoxide
by: Hodgson, D, et al.
Published: (2003) -
Functionalised bicyclic alcohols by enantioselective alpha-deprotonation-rearrangement of meso-epoxides
by: Hodgson, D, et al.
Published: (2001) -
Enantioselective alpha-deprotonation of epoxides.
by: Hodgson, D
Published: (2001) -
Enantioselective synthesis of epoxides by alpha-deprotonation--electrophile trapping of achiral epoxides.
by: Hodgson, D, et al.
Published: (2003)