The synthesis of a 5,7-membered fused-ring compound by a tandem pummerer rearrangement and intramolecular [4+3] cycloaddition

被引：23
|
作者：
Hu, YH [1 ]
Ou, LG [1 ]
Bai, DL [1 ]
机构：
[1] Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 200031, Peoples R China
来源：
TETRAHEDRON LETTERS | 1999年 / 40卷 / 03期
关键词：
D O I：
10.1016/S0040-4039(98)02404-6
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A 5, 7-membered fused-ring compound with a functionalized angular substituent, 8-methoxy-8a alpha-methoxymethyl-7-phenylthio-1, 2, 3, 6-tehahydro-3a alpha, 6 beta-epoxyazulene, was synthesized via a tandem Pummerer rearrangement and intramolecular [4+3] cycloaddition. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码：545 / 548
页数：4
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