Literature DB >> 15307762

Indium(I) iodide-promoted cleavage of diaryl diselenides and disulfides and subsequent condensation with alkyl or acyl halides. One-pot efficient synthesis of diorganyl selenides, sulfides, selenoesters, and thioesters.

Brindaban C Ranu1, Tanmay Mandal.   

Abstract

Diphenyl diselenides and disulfides undergo facile cleavages by indium(I) iodide and the corresponding generated selenate and thiolate anions condense in situ with alkyl or acyl halides present in the reaction mixture. Thus, a simple, efficient, and general procedure has been developed for the synthesis of unsymmetrical diorganyl selenides, sulfides (thioethers), selenoesters, and thioesters by this one-pot reaction at room temperature. Copyright 2004 American Chemical Society

Entities:  

Year:  2004        PMID: 15307762     DOI: 10.1021/jo0493727

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Atom Efficient Preparation of Zinc Selenates for the Synthesis of Selenol Esters under "On Water" Conditions.

Authors:  Luca Sancineto; Jaqueline Pinto Vargas; Bonifacio Monti; Massimiliano Arca; Vito Lippolis; Gelson Perin; Eder Joao Lenardao; Claudio Santi
Journal:  Molecules       Date:  2017-06-08       Impact factor: 4.411

2.  Role of TBATB in nano indium oxide catalyzed C-S bond formation.

Authors:  Prasanta Gogoi; Sukanya Hazarika; Pranjit Barman
Journal:  Sci Rep       Date:  2015-09-29       Impact factor: 4.379

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.