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Efficient Synthesis of Polyfunctionalized Benzenes in Water via Persulfate-promoted Benzannulation of α,β-Unsaturated Compounds and Alkynes
Published on: December 16, 2019
Bifunctionalization of styrene through ring-opening-recombination strategy of phenylpropathiazole salt
Yongbo Fan1, Shengting Xu1, Xinxin Cai1
1School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, China. chenxiuwen2010@126.com.
Abstract:
By opening the ring of a benzothiazole salt, we provide a sulfur source for the bifunctional reaction of styrene. The ring-opening-recombination reaction of the benzothiazole salt simultaneously constructs new C-S, C-O, and CO bonds after C-S bond breaking. The reaction proceeds in green solvents, requires no transition metal catalyst, and is compatible with many functional groups.
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