化学
区域选择性
二硒醚
硫黄
硒
组合化学
立体化学
有机化学
催化作用
作者
Jin Yin,Peng Chen,Le‐Wei Miao,Jie Wang,Yijun Jiang
标识
DOI:10.1002/ejoc.202300290
摘要
Abstract The first direct and selective 3,6‐di‐thiolation and 3,6‐di‐selenylation of carbazoles using diaryl disulfides/diselenide as the sulfur/selenium source were demonstrated. This simple, general, and efficient method could deliver a wide range of 3,6‐di‐sulfenyl‐carbazoles and 3,6‐di‐selenyl‐carbazoles from readily available starting materials with high regioselectivity in an easily‐operated one‐step reaction via a Ag/K 2 S 2 O 8 ‐mediated protocol.
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