Literature DB >> 22951492

An efficient synthesis of 2-bromo(chloro)-3-selenyl(sulfenyl)indoles via tandem reactions of 2-(gem-dibromo(chloro)vinyl)anilines with diselenides(disulfides).

Jie Liu1, Pinhua Li, Wei Chen, Lei Wang.   

Abstract

A novel and efficient synthesis of 2-bromo(chloro)-3-selenyl(sulfenyl)indoles through tandem reactions of 2-(gem-dibromo(chloro)vinyl)-N-methylsulfonylanilines with diselenides and disulfides in the presence of t-BuOLi and I(2) (10 mol%) in DMSO was developed. The reactions generated the desired products in good yields with high regio-selectivity under transition-metal-free conditions in one-pot.

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Year:  2012        PMID: 22951492     DOI: 10.1039/c2cc34800d

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Silver-catalyzed direct thiolation of quinones by activation of aryl disulfides to synthesize quinonyl aryl thioethers.

Authors:  Cheng Zhang; Jesse McClure; C James Chou
Journal:  J Org Chem       Date:  2015-04-27       Impact factor: 4.354

Review 2.  Synthetic strategies for aryl/heterocyclic selenides and tellurides under transition-metal-catalyst free conditions.

Authors:  Debasish Kundu
Journal:  RSC Adv       Date:  2021-02-10       Impact factor: 3.361

3.  A selenium-based ionic liquid as a recyclable solvent for the catalyst-free synthesis of 3-selenylindoles.

Authors:  Everton G Zimmermann; Samuel Thurow; Camilo S Freitas; Samuel R Mendes; Gelson Perin; Diego Alves; Raquel G Jacob; Eder J Lenardão
Journal:  Molecules       Date:  2013-04-05       Impact factor: 4.411

  3 in total

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