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引用次数: 0

摘要

报告了一种钯/手性 N,N′-二磺酰基双咪唑啉(Bim)催化的芳基硼酸与异喹啉-1,3,4-三酮衍生酮亚胺的不对称加成反应,从而生成了一系列具有一个季碳-氨基官能团的官能化异喹啉-1,3(2H,4H)-二酮,收率良好至极佳,大多数情况下ee值≥95%。该反应与两种底物范围都有显著的兼容性,为手性杂环 α-叔胺提供了一个高度对映选择性的入口。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pd(II)/N,N′-Disulfonyl bisimidazoline-catalyzed asymmetric arylation of isoquinoline-1,3,4-trione-derived ketimines

Pd(II)/N,N′-Disulfonyl bisimidazoline-catalyzed asymmetric arylation of isoquinoline-1,3,4-trione-derived ketimines

Pd(II)/N,N′-Disulfonyl bisimidazoline-catalyzed asymmetric arylation of isoquinoline-1,3,4-trione-derived ketimines

A palladium/chiral N,N′-disulfonyl bisimidazoline (Bim)-catalyzed asymmetric addition of arylboronic acids to isoquinoline-1,3,4-trione-derived ketimines is reported, leading to the generation of a series of functionalized isoquinoline-1,3(2H,4H)-diones bearing one quaternary carbon-amino functionality in good to excellent yields with ≥95% ee in most cases. The reaction has remarkable compatibility with both substrate scopes, providing a highly enantioselective entry to chiral heterocyclic α-tertiary amines.

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