Suppr超能文献

辛可宁生物碱螺酰胺/AgOAc 协同催化的异氰酸酯和环状三氟甲基亚胺的非对映选择性和对映选择性 Mannich/环化级联反应。

Cinchona alkaloid squaramide/AgOAc cooperatively catalyzed diastereo- and enantioselective Mannich/cyclization cascade reaction of isocyanoacetates and cyclic trifluoromethyl ketimines.

机构信息

Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology , Shanghai 200237, P.R. China.

出版信息

Org Lett. 2014 Sep 5;16(17):4566-9. doi: 10.1021/ol502123z. Epub 2014 Aug 21.

Abstract

An efficient diastereo- and enantioselective Mannich-type/cyclization cascade reaction of α-substituted isocyanoacetates and cyclic trifluoromethyl ketimines cooperatively catalyzed by cinchona alkaloid-derived multi-hydrogen-bonding donor squaramide and AgOAc has been investigated, affording the optically active trifluoromethyl-substituted tetrahydroimidazo[1,5-c]quinazoline derivatives in excellent yields (up to 99%) and good to excellent stereoselectivities (up to >15:1 dr, up to 98% ee) under mild conditions.

摘要

一种高效的非对映选择性和对映选择性的 Mannich 型/环化级联反应,由金鸡纳生物碱衍生的多氢键供体双噁唑啉和 AgOAc 共同催化α-取代异氰基乙酸酯和环状三氟甲基亚胺,可以得到光学活性的三氟甲基取代的四氢咪唑并[1,5-c]喹唑啉衍生物,产率优异(高达 99%),立体选择性好至优秀(高达 >15:1 dr,高达 98%ee),条件温和。

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