N-acylation of 1,3-dimethyl-6-aminouracils. A reversal in the regiospecificity of an electrophilic substitution induced by an intramolecular proton-transfer-Reference-Cited by-同舟云学术

N-acylation of 1,3-dimethyl-6-aminouracils. A reversal in the regiospecificity of an electrophilic substitution induced by an intramolecular proton-transfer

Published:1984-07 Issue:4 Volume:21 Page:1129-1134
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:

Author:

Bernier Jean-Luc,HÉnichart Jean-Pierre,Warin Vincent

Publisher

Wiley

Subject

Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.5570210440/fullpdf

Reference43 articles.

1. a A. G. Cooke, “Enamines: Their Synthesis, Structure and Reactions”, M. Dekker, ed, New York, 1969, and references cited therein;

2. Chemistry of Heterocyclic Compounds

3. Reactions of 1,3-Dimethyl-5,6-diaminouracil

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2. STUDY ON THE RENAL AND CARDIOVASCULAR ACTIVITIES OF AMINOURACIL DERIVATIVES;Pharmaceutical Research;1989

3. Reactions of Annular Nitrogens of Azines with Electrophiles;Advances in Heterocyclic Chemistry;1988

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5. ChemInform Abstract: N-ACYLATION OF 1,3-DIMETHYL-6-AMINOURACILS. A REVERSAL IN THE REGIOSPECIFICITY OF AN ELECTROPHILIC SUBSTITUTION INDUCED BY AN INTRAMOLECULAR PROTON-TRANSFER;Chemischer Informationsdienst;1985-03-26