Facile Transformation of 2-azetidinones to 2-piperidones:: Application to the synthesis of the indolizidine skeleton and (8S,8aS)-perhydro-8-indolizinol

被引:42
作者
Lee, HK [1 ]
Chun, JS [1 ]
Pak, CS [1 ]
机构
[1] Korea Res Inst Chem Technol, Bioorgan Sci Div, Taejon 305606, South Korea
关键词
D O I
10.1021/jo026817n
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The highly functionalized bicyclic lactam 7 was prepared from diolefinic-2-piperidone 18 by the use of ruthenium-catalyzed RCM, and in turn, 18 was derived via a two-carbon addition process from readily accessible 4-olefinic-2-azetidinone 13. Bicyclic lactams 7 and 20 could serve as potentially valuable intermediates for the chiral synthesis of various hydroxylated indolizidine alkaloids as exemplified by the synthesis of (8S,8aS)-perhydro-8-indolizinol 19.
引用
收藏
页码:2471 / 2474
页数:4
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