Literature DB >> 26052796

Tetrabutylammonium iodide-catalyzed oxidative coupling of enamides with sulfonylhydrazides: synthesis of β-keto-sulfones.

Yucai Tang1, Ye Zhang, Kaifeng Wang, Xiaoqing Li, Xiangsheng Xu, Xiaohua Du.   

Abstract

A facile synthetic route towards pharmaceutically interesting β-keto-sulfone derivatives by tetrabutylammonium iodide (TBAI)/tert-butyl hydroperoxide (TBHP) mediated oxidative coupling of readily prepared enamides with economical sulfonylhydrazides is described. The corresponding β-keto-sulfone compounds were obtained in moderate to good yields. The present method is metal-free and base-free and shows tolerance to a variety of functional groups.

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Year:  2015        PMID: 26052796     DOI: 10.1039/c5ob00742a

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


  3 in total

1.  An efficient access to β-ketosulfones via β-sulfonylvinylamines: metal-organic framework catalysis for the direct C-S coupling of sodium sulfinates with oxime acetates.

Authors:  Tuong A To; Chau B Tran; Ngoc T H Nguyen; Hai H T Nguyen; Anh T Nguyen; Anh N Q Phan; Nam T S Phan
Journal:  RSC Adv       Date:  2018-05-14       Impact factor: 4.036

2.  Synthesis of trifluoromethyl-containing isoindolinones from tertiary enamides via a cascade radical addition and cyclization process.

Authors:  Hui Yu; Mingdong Jiao; Xiaowei Fang; Pengfei Xuan
Journal:  RSC Adv       Date:  2018-07-03       Impact factor: 3.361

3.  Facile Electrochemical Intramolecular Amination of Urea-Tethered Terminal Alkenes for the Synthesis of Cyclic Ureas.

Authors:  Nisar Ahmed; Saira Khatoon
Journal:  ChemistryOpen       Date:  2018-07-09       Impact factor: 2.911

  3 in total

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