Rh(II)催化吡啶三唑和硫化物的高效西格玛重排反应

Yuting Chen , Guanghui Lv , Zhiyang Li , Meiling Ye , Tianle Huang , Li Hai , Yong Wu
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引用次数: 0

摘要

研究了铑(II)催化的吡啶三唑与硫化物之间的[2,3]-和[1,2]-异相重排反应。在这种反应中,利用吡啶三唑作为碳烯前体,可以有效地构建 C(sp3)-S 和 C(sp3)-Se 键,具有广泛的底物范围和很强的官能团耐受性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Rh(II) catalyzed efficient sigmatropic rearrangement reaction of pyridotriazoles and sulfides

Rh(II) catalyzed efficient sigmatropic rearrangement reaction of pyridotriazoles and sulfides

Rh(II) catalyzed efficient sigmatropic rearrangement reaction of pyridotriazoles and sulfides

The [2,3]- and [1,2]-sigmatropic rearrangement reactions between pyridotriazoles and sulfides catalyzed by rhodium(II) were investigated. The utilization of pyridotriazoles as the carbene precursors in this kind of reaction efficiently constructed the C(sp3)-S and C(sp3)-Se bond with broad substrate scope and great functional group tolerance.

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