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Synlett 1996; 1996(12): 1206-1208
DOI: 10.1055/s-1996-5705
DOI: 10.1055/s-1996-5705
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.
A New and Convenient Access to N-Alkoxypyridine-2(1H)-thiones
Further Information
Publication History
Publication Date:
31 December 2000 (online)
The reaction of 2,2’dithiopyridine-1,1’-dioxide (6) and alkyl, allyl, or benzyl alcohols in the presence of a tertiary phosphine provides a new and versatile method for the synthesis of thiohydroxamic acid O-esters 8.
pyridinethiones - thiohydroxamic acid - alkylation