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Synthesis of 3-Substituted Aryl[4,5]isothiazoles through an All-Heteroatom Wittig-Equivalent Process
Organic Letters ( IF 4.9 ) Pub Date : 2016-05-24 00:00:00 , DOI: 10.1021/acs.orglett.6b01338
Fanghui Xu 1 , Yuan Chen 1 , Erkang Fan 2 , Zhihua Sun 1
Affiliation  

Extending the previous use of tert-butyl sulfoxide as the sulfinyl source, intramolecular sulfinylation of sulfonamides was successfully performed. The resulting sulfinimides were not isolated and instead were believed to go through an all-heteroatom Wittig-equivalent process to eventually afford aryl[4,5]isothiazoles in high yields.

中文翻译:

全杂原子Wittig等效法合成3-取代的芳基[4,5]异噻唑

扩展了以前使用丁基亚砜作为亚磺酰基的来源,磺酰胺的分子内亚磺酰基化成功地进行了。没有分离得到的亚磺酰亚胺,而是据信经历了全杂原子维蒂希当量过程,最终以高收率获得了芳基[4,5]异噻唑。
更新日期:2016-05-24
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