4.4 Article

Synthesis of novel pentacyclic thiopyrano indole-annulated benzo-δ-sultone derivatives via a domino Knoevenagel-hetero-Diels-Alder reaction in water

期刊

TETRAHEDRON LETTERS
卷 54, 期 21, 页码 2685-2689

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2013.03.070

关键词

Knoevenagel-hetero-Diels-Alder; Domino reaction; Indoline-2-thiones; Aqueous medium; Benzo-delta-sultones; Thiopyrano indole

向作者/读者索取更多资源

An efficient synthesis of novel pentacyclic thiopyrano indole-annulated benzo-delta-sultone derivatives is achieved via intramolecular domino Knoevenagel-hetero-Diels-Alder reaction of 2-formylphenyl (E)-2-phenylethenyl sulfonates and indoline-2-thiones in aqueous medium. The products are formed in good yields with high regio- and stereoselectivity. (c) 2013 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