A novel and efficient 4-oxothiazolidine-1,2-dithiole rearrangement induced by Lawesson's reagent

Markovic, R
Baranac-Stojanović, Marija
Jovetic, S

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Publication date

January 2003

DOI

10.1016/S0040-4039(03)01721-0

Publisher

Pergamon-Elsevier Science Ltd, Oxford

Journal

issn:0040-4039

Abstract

Functionalized 1,2-dithioles have been synthesized by a ring opening-closing process of 5-substituted- and 5-unsubstituted-2-alkylidene-4-oxothiazolidines with Lawesson's reagent. The C-13 NMR data confirmed the meso-ionic structure of these aromatic-type 1,2-dithioles. (C) 2003 Elsevier Ltd. All rights reserved

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A novel and efficient 4-oxothiazolidine-1,2-dithiole rearrangement induced by Lawesson's reagent

Abstract

Extracted data

A novel and efficient 4-oxothiazolidine-1,2-dithiole rearrangement induced by Lawesson's reagent

Abstract

Extracted data

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