Reaction of 1-tosyl-2,2-dichloroenamines with the Lawesson’s reagent View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2012-05

AUTHORS

K. V. Turov, T. K. Vinogradova, E. B. Rusanov, V. S. Brovarets

ABSTRACT

In the reaction of the available 1-tosyl-2,2-dihlorenamides with the Lawesson’s reagent the derivatives of 4-tosyl-1,3-thiazole were shown to form containing a labile chlorine atom at the C5 position. This fact was used for the synthesis of a number of the previously unknown bifunctionally substituted 4,5-thiazoles.

PAGES

848-852

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070363212050076

DOI

http://dx.doi.org/10.1134/s1070363212050076

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1029207597


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