About: Chemistry of Tetrathiomolybdate: Aziridine Ring Opening Reactions andFacile Synthesis of Interesting Sulfur Heterocycles

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_37/w
Subject	Communication
Title	Chemistry of Tetrathiomolybdate: Aziridine Ring Opening Reactions andFacile Synthesis of Interesting Sulfur Heterocycles
has manifestation of work	http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_37/101021ja052969z/m/print http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_37/101021ja052969z/m/web
related by	http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_37/101021ja052969z/authorship/1 http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_37/101021ja052969z/authorship/3 http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_37/101021ja052969z/authorship/2
Author	Sureshkumar Devarajulu Koutha Srinivasa Murthy Chandrasekaran Srinivasan
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.
article type	rapid-communication
is part of this journal	Journal of the American Chemical Society

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