芳基
磺酰
化学
试剂
催化作用
硫黄
基质(水族馆)
有机化学
溶剂
组合化学
胺化
烷基
海洋学
地质学
作者
Yutong Yuan,Jing He,Xiaowei Ma,Sheng Han,Yan Liu
出处
期刊:Molecules
[MDPI AG]
日期:2024-05-21
卷期号:29 (11): 2411-2411
标识
DOI:10.3390/molecules29112411
摘要
An iodophor-catalyzed direct disulfenylation of amino naphthalenes with aryl sulfonyl hydrazines in water was developed. A series of aryl sulfides were obtained in moderate to excellent yields. The advantages of this green protocol were the simple reaction conditions (metal-free, water as the solvent, under air), the odorless and easily available sulfur reagent, the broad substrate scope, and gram-scale synthesis. Moreover, the potential application of aryl sulfides was exemplified by further transformations.
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