Organic and Medicinal Chemistry Division, CSIR-Indian Institute of Chemical Biology, 4-Raja S. C. Mullick Road, Jadavpur, Kolkata 700032, India.
Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, Uttar Pradesh 201002, India.
Chem Commun (Camb). 2022 Feb 24;58(17):2902-2905. doi: 10.1039/d1cc07143b.
A straightforward strategy for direct incorporation of sulfonyl units into a xanthene moiety for accessing xanthen-9-sulfone derivatives in good to excellent yields has been established metal-free radical-radical cross-coupling reaction of xanthenes and sulfonyl hydrazides. Using easily accessible starting materials, this methodology proceeds efficiently with a high degree of functional group compatibility and with a wide scope of both xanthenes and sulfonyl hydrazides under operationally simple reaction conditions. Mechanistic investigations revealed that sulfonyl radicals could be generated from sulfonyl hydrazides in the presence of TBHP under an oxygen atmosphere.
建立了一种直接将磺酰基单元引入呫吨部分的简便策略,用于在无金属自由基-自由基交叉偶联反应中以良好至优秀的收率获得呫吨-9-砜衍生物。该方法使用易得的起始原料,在操作简单的反应条件下,对多种呫吨和磺酰肼具有高效、高官能团兼容性和广泛的适用性。机理研究表明,在氧气气氛下,TBHP 存在时,磺酰基肼可以生成磺酰基自由基。