An approach to the synthesis of furanoheliangolides through Diels-Alder reactions

被引：6
|
作者：
Constantino, Mauricio Gomes [1 ]
Aragao, Valquiria [1 ]
da Silva, Gil Valdo Jose [1 ]
机构：
[1] Univ Sao Paulo, Dept Quim, Fac Filosofia Ciencias & Letras Ribeirao Pret, BR-14040901 Ribeirao Preto, SP, Brazil
来源：
TETRAHEDRON LETTERS | 2008年 / 49卷 / 08期
基金：
巴西圣保罗研究基金会;
关键词：
synthesis; natural products; furanoheliangolides; Diels-Alder reactions;
D O I：
10.1016/j.tetlet.2007.12.079
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The core structure of the natural sesquiterpene lactones furanoheliangolides, an 11-oxabicyclo[6.2.1]undecane system, was synthesized through a pathway involving two Diels-Alder reactions. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码：1393 / 1395
页数：3
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