4.4 Article

Domino-Knoevenagel-hetero-Diels-Alder reactions: an efficient one-step synthesis of indole-annulated thiopyranobenzopyran derivatives

期刊

TETRAHEDRON LETTERS
卷 50, 期 27, 页码 3889-3891

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2009.04.054

关键词

Domino-intramolecular; Knoevenagel-hetero-Diels-Alder reactions; O-Allylated salicylaldehydes; 1-Methylindoline-2-thione; One-step synthesis

资金

  1. CSIR (New Delhi)
  2. DST (New Delhi)

向作者/读者索取更多资源

Rapid one-step synthesis of hitherto unreported indole-annulated pentacyclic heterocycles containing oxygen, nitrogen, and sulfur has been described by domino-Knoevenagel-hetero-Diels-Alder reaction. The reaction sequence provides a route to the synthesis of a novel type of polyheterocycles in excellent yields with high stereoselectivity. (c) 2009 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据