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
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
收藏
页码:153 / 156
页数:4
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