Literature DB >> 29115334

Efficient dehydrative alkylation of thiols with alcohols catalyzed by alkyl halides.

Yaqi Yang1, Zihang Ye, Xu Zhang, Yipeng Zhou, Xiantao Ma, Hongen Cao, Huan Li, Lei Yu, Qing Xu.   

Abstract

Alcohols can be efficiently converted into the useful thioethers by a transition metal- and base-free dehydrative S-alkylation reaction with thiols or disulfides by employing alkyl halides as the effective catalyst. This simple and efficient method is a green and practical way for the preparation of thioethers, as it tolerates a wide range of substrates such as aryl and alkyl thiols, as well as benzylic, allylic, secondary, tertiary, and even the less reactive aliphatic alcohols.

Entities:  

Year:  2017        PMID: 29115334     DOI: 10.1039/c7ob02461d

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

1.  Hydrogen-bond donor and acceptor cooperative catalysis strategy for cyclic dehydration of diols to access O-heterocycles.

Authors:  Huan Wang; Yanfei Zhao; Fengtao Zhang; Zhengang Ke; Buxing Han; Junfeng Xiang; Zhenpeng Wang; Zhimin Liu
Journal:  Sci Adv       Date:  2021-05-26       Impact factor: 14.136

2.  Benzyl thioether formation merging copper catalysis.

Authors:  Bing Xu; Ying Lin; Yang Ye; Li Xu; Tian Xie; Xiang-Yang Ye
Journal:  RSC Adv       Date:  2021-12-23       Impact factor: 3.361

3.  B(C6F5)3 catalyzed direct nucleophilic substitution of benzylic alcohols: an effective method of constructing C-O, C-S and C-C bonds from benzylic alcohols.

Authors:  Shan-Shui Meng; Qian Wang; Gong-Bin Huang; Li-Rong Lin; Jun-Ling Zhao; Albert S C Chan
Journal:  RSC Adv       Date:  2018-09-03       Impact factor: 3.361

  3 in total

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