Suppr超能文献

金(I)催化的二烯炔分子内环丙烷化反应。

Gold(I)-catalyzed intramolecular cyclopropanation of dienynes.

作者信息

Nieto-Oberhuber Cristina, López Salomé, Muñoz M Paz, Jiménez-Núñez Eloísa, Buñuel Elena, Cárdenas Diego J, Echavarren Antonio M

机构信息

Institute of Chemical Research of Catalonia (ICIQ), Av. Països Catalans 16, 43007 Tarragona, Spain.

出版信息

Chemistry. 2006 Feb 8;12(6):1694-702. doi: 10.1002/chem.200501089.

Abstract

Gold(I) complexes are the most active catalysts for the biscyclopropanation of dienynes to form tetracyclic compounds. PtII and ZnII are also able to promote the biscyclopropanation, although less efficiently. The configurations obtained in all cases with the use of gold(I) catalysts can be explained by the pathway proceeding through anti cyclopropyl gold carbenes. Similar intermediates are most probably involved in reactions catalyzed by RuII and PtII. Two different cyclopropanation pathways have been found; they depend on the structures of the cyclopropyl gold carbenes (anti or syn) and the relative arrangements of the metal carbenes and the alkenes.

摘要

金(I)配合物是二烯炔双环丙烷化反应生成四环化合物最有效的催化剂。尽管效率较低,PtII和ZnII也能够促进双环丙烷化反应。在所有使用金(I)催化剂的情况下所得到的构型可以通过经由反式环丙基金卡宾的反应途径来解释。最有可能的是,RuII和PtII催化的反应中也涉及类似的中间体。已发现两种不同的环丙烷化途径;它们取决于环丙基金卡宾的结构(反式或顺式)以及金属卡宾与烯烃的相对排列。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验