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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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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
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author Liu, Teng
Liu, Jianjun
Xia, Shubiao
Meng, Jie
Shen, Xianfu
Zhu, Xiufang
Chen, Wenchang
Sun, Chengke
Cheng, Feixiang
author_facet Liu, Teng
Liu, Jianjun
Xia, Shubiao
Meng, Jie
Shen, Xianfu
Zhu, Xiufang
Chen, Wenchang
Sun, Chengke
Cheng, Feixiang
author_sort Liu, Teng
collection PubMed
description [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.
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spelling pubmed-66412502019-08-27 Catalyst-Free 1,6-Conjugate Addition/Aromatization/Sulfonylation of para-Quinone Methides: Facile Access to Diarylmethyl Sulfones Liu, Teng Liu, Jianjun Xia, Shubiao Meng, Jie Shen, Xianfu Zhu, Xiufang Chen, Wenchang Sun, Chengke Cheng, Feixiang ACS Omega [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. American Chemical Society 2018-02-02 /pmc/articles/PMC6641250/ /pubmed/31458470 http://dx.doi.org/10.1021/acsomega.7b01745 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Liu, Teng
Liu, Jianjun
Xia, Shubiao
Meng, Jie
Shen, Xianfu
Zhu, Xiufang
Chen, Wenchang
Sun, Chengke
Cheng, Feixiang
Catalyst-Free 1,6-Conjugate Addition/Aromatization/Sulfonylation of para-Quinone Methides: Facile Access to Diarylmethyl Sulfones
title Catalyst-Free 1,6-Conjugate Addition/Aromatization/Sulfonylation of para-Quinone Methides: Facile Access to Diarylmethyl Sulfones
title_full Catalyst-Free 1,6-Conjugate Addition/Aromatization/Sulfonylation of para-Quinone Methides: Facile Access to Diarylmethyl Sulfones
title_fullStr Catalyst-Free 1,6-Conjugate Addition/Aromatization/Sulfonylation of para-Quinone Methides: Facile Access to Diarylmethyl Sulfones
title_full_unstemmed Catalyst-Free 1,6-Conjugate Addition/Aromatization/Sulfonylation of para-Quinone Methides: Facile Access to Diarylmethyl Sulfones
title_short Catalyst-Free 1,6-Conjugate Addition/Aromatization/Sulfonylation of para-Quinone Methides: Facile Access to Diarylmethyl Sulfones
title_sort catalyst-free 1,6-conjugate addition/aromatization/sulfonylation of para-quinone methides: facile access to diarylmethyl sulfones
url 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
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