Suppr超能文献

室温下在水中合成α-羰基-α'-亚磺酰基锍叶立德

Synthesis of α-Carbonyl-α'-sulfenyl Sulfoxonium Ylides in Water at Room Temperature.

作者信息

Tian Haoyu, Wang Qinghe, Wei Wenyan, Chen Yan, Zhong Xia, Yao Guiwei, Chen Xun, Zhao Guangkuan, Kong Dulin

机构信息

Engineering Research Center of Tropical Medicine Innovation and Transformation of Ministry of Education, International Joint Research Center of Human-machine Intelligent Collaborative for Tumor Precision Diagnosis and Treatment of Hainan Province, Hainan Provincial Key Laboratory of Research and Development on Tropical Herbs, School of Pharmaceutical Sciences, Hainan Medical University, Haikou 571199, Hainan Province, P.R. China.

Venturepharm Pharmaceuticals (Hainan) Co., Ltd., No. 279, Nanhai Avenue, Haikou 570100, Hainan Province, China.

出版信息

J Org Chem. 2024 Nov 1;89(21):15523-15528. doi: 10.1021/acs.joc.4c01592. Epub 2024 Oct 19.

Abstract

An efficient synthesis of α-carbonyl-α'-sulfenyl sulfoxonium ylides through a KIO-promoted cross-dehydrogenative coupling reaction of aryl thiols and α-carbonyl sulfoxonium ylides in an aqueous medium at room temperature has been described. The α-carbonyl sulfoxonium ylides and aryl thiols adorned with various functional groups were well-tolerated and afforded moderate to high yields of α-carbonyl-α-sulfenyl sulfoxonium ylide derivatives. Finally, by converting synthesized ylide into other valuable compounds, we demonstrated the practicality of this synthetic method.

摘要

描述了一种在室温下于水性介质中通过KIO促进的芳基硫醇与α-羰基锍叶立德的交叉脱氢偶联反应高效合成α-羰基-α'-亚磺酰基锍叶立德的方法。带有各种官能团的α-羰基锍叶立德和芳基硫醇具有良好的耐受性,并且以中等至高产率得到α-羰基-α-亚磺酰基锍叶立德衍生物。最后,通过将合成的叶立德转化为其他有价值的化合物,我们证明了这种合成方法的实用性。

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