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Catalyst-Free 1,6-Conjugate Addition/Aromatization/Sulfonylation of para-Quinone Methides: Facile Access to Diarylmethyl Sulfones

[Image: see text] An efficient, catalyst-free strategy to construct diarylmethyl sulfones via 1,6-conjugate addition/aromatization/sulfonylation reaction of para-quinone methides with sulfonyl hydrazides under mild and environmentally benign conditions has been developed. The established protocol pr...

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Detalles Bibliográficos
Autores principales: Liu, Teng, Liu, Jianjun, Xia, Shubiao, Meng, Jie, Shen, Xianfu, Zhu, Xiufang, Chen, Wenchang, Sun, Chengke, Cheng, Feixiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641250/
https://www.ncbi.nlm.nih.gov/pubmed/31458470
http://dx.doi.org/10.1021/acsomega.7b01745
Descripción
Sumario:[Image: see text] An efficient, catalyst-free strategy to construct diarylmethyl sulfones via 1,6-conjugate addition/aromatization/sulfonylation reaction of para-quinone methides with sulfonyl hydrazides under mild and environmentally benign conditions has been developed. The established protocol provided a highly chemo- and regioselectivity synthesis of a diverse array of novel diarylmethyl sulfones with excellent yields, and the reaction could be scaled up.