Literature DB >> 16159244

Chemistry of tetrathiomolybdate: aziridine ring opening reactions and facile synthesis of interesting sulfur heterocycles.

Devarajulu Sureshkumar1, Srinivasa Murthy Koutha, Srinivasan Chandrasekaran.   

Abstract

Benzyltriethylammonium tetrathiomolybdate, [BnEt3N]2MoS4, has been used successfully to effect ring opening of aziridines in a regiospecific and stereospecific manner under mild reaction conditions without the use of Lewis acid catalyst. Utility of this reagent in tandem and multistep processes in a one-pot operation for the synthesis of various novel sulfur heterocycles in very good yield is also reported.

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Year:  2005        PMID: 16159244     DOI: 10.1021/ja052969z

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  3 in total

1.  Highly efficient synthesis of alkyl and aryl primary thiocarbamates and dithiocarbamates under metal- and solvent-free conditions.

Authors:  Ali Reza Sardarian; Iman Dindarloo Inaloo; Ali Reza Modarresi-Alam
Journal:  Mol Divers       Date:  2018-06-12       Impact factor: 2.943

2.  Crystal structure and Hirshfeld surface analysis of N,N'-[ethane-1,2-diylbis(-oxy)]bis-(4-methyl-benzene-sulfonamide).

Authors:  Seher Meral; Sevgi Kansiz; Necmi Dege; Aysen Alaman Agar; Galyna G Tsapyuk
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2019-01-01

3.  Convenient and efficient synthesis of functionalized unsymmetrical Z-alkenyl disulfanes.

Authors:  M Musiejuk; J Doroszuk; D Witt
Journal:  RSC Adv       Date:  2018-03-07       Impact factor: 3.361

  3 in total

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