TOTAL SYNTHESIS OF (+) MONOMORINE-I FROM CHIRAL CYCLIC BETA-ENAMINO ESTER

被引：58

作者：

SALIOU, C ^{[1
]}

FLEURANT, A ^{[1
]}

CELERIER, JP ^{[1
]}

LHOMMET, G ^{[1
]}

机构：

[1] UNIV PARIS 06, CHIM HETEROCYCLES LAB, CNRS, 4 PL JUSSIEU, F-75252 PARIS 05, FRANCE

来源：

TETRAHEDRON LETTERS | 1991年 / 32卷 / 28期

关键词：

(S)-PYROGLUTAMIC ACID; CYCLIC BETA-ENAMINO ESTER; CYCLIC BETA-AMINO ALCOHOL; STABILIZED YLIDS; ENANTIOSPECIFIC IMINIUM REDUCTION; ENANTIOSELECTIVE TOTAL SYNTHESIS; STEREOSELECTIVE SYNTHESIS; (+/-)-MONOMORINE-I; (+)-MONOMORINE-I;

D O I：

10.1016/S0040-4039(00)92707-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

We describe the total synthesis of (+) Monomorine I 1 and the preparation of cis-2,5-disubstituted functionalized pyrrolidines via cyclic beta-enamino esters 4, starting from (S)-pyroglutamic acid.

引用

页码：3365 / 3368

页数：4

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