Highly Enantioselective Approach to Indolizidines: Preparation of (+)-(1S,8aS)-1-Hydroxyindolizidine and (−)-Slaframine
摘要:
A highly stereoselective approach to (-)-slaframine and its probable biosynthetic precursor (+)-(1S,8aS)-1-hydroxyindolizidine has been developed based on a diastereofacially selective cycloaddition of dichloroketene with achiral dienol ether.
Highly Enantioselective Approach to Indolizidines: Preparation of (+)-(1S,8aS)-1-Hydroxyindolizidine and (−)-Slaframine
摘要:
A highly stereoselective approach to (-)-slaframine and its probable biosynthetic precursor (+)-(1S,8aS)-1-hydroxyindolizidine has been developed based on a diastereofacially selective cycloaddition of dichloroketene with achiral dienol ether.
Highly Enantioselective Approach to Indolizidines: Preparation of (+)-(1<i>S</i>,8a<i>S</i>)-1-Hydroxyindolizidine and (−)-Slaframine
作者:Mehrnaz Pourashraf、Philippe Delair、Martin O. Rasmussen、Andrew E. Greene
DOI:10.1021/jo0005621
日期:2000.10.1
A highly stereoselective approach to (-)-slaframine and its probable biosynthetic precursor (+)-(1S,8aS)-1-hydroxyindolizidine has been developed based on a diastereofacially selective cycloaddition of dichloroketene with achiral dienol ether.