The enantiospecific total synthesis of norsuaveoline

被引：23

作者：

Wang, T ^{[1
]}

Yu, P ^{[1
]}

Li, J ^{[1
]}

Cook, JM ^{[1
]}

机构：

[1] Univ Wisconsin, Dept Chem, Milwaukee, WI 53201 USA

来源：

TETRAHEDRON LETTERS | 1998年 / 39卷 / 44期

关键词：

D O I：

10.1016/S0040-4039(98)01788-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Norsuaveoline 1a has been synthesized enantiospecifically in 28% overall yield from commercially available D-(+)-tryptophan methyl ester via the asymmetric Pictet-Spengler reaction and a stereocontrolled oxy-anion Cope rearrangement as key steps. (C) 1998 Elsevier Science Ltd. All rights reserved.

引用

页码：8009 / 8012

页数：4

共 12 条

[1]

Bi Y., 1993, STUDIES NATURAL PROD, V13, P383

[2]

COOK JM, 1971, THESIS U MICHIGAN

[3]

Isidro N., 1967, J PHILLIPINE PHARM A, V53, P8

[4]

LI J, UNPUB THIS DEGRADATI