Synthetic studies on sarcodictyins and eleutherobin: Synthesis of fully functionalized cyclization precursors

被引：44

作者：

Ceccarelli, S

Piarulli, U

Gennari, C

机构：

[1] Univ Milan, Ctr CNR, Dipartimento Chim Organ & Ind, I-20133 Milan, Italy

[2] Univ Studi Insubria, Ist Sci Mat Fis & Chim, I-22100 Como, Italy

来源：

TETRAHEDRON LETTERS | 1999年 / 40卷 / 01期

关键词：

antitumour compounds; asymmetric synthesis; marine metabolites; Wittig reactions;

D O I：

10.1016/S0040-4039(98)80045-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Unprecedented synthetic transformations were demonstrated during the preparation of fully functionalized cyclization precursors of type 2, in a synthetic approach to sarcodictyin A and B (1a,b) and eleutherobin (1c). (C) 1998 Elsevier Science Ltd. All rights reserved.

引用

页码：153 / 156

页数：4

共 31 条

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