Partially hydrogenated 2-amino[1,2,4]triazolo[1,5-a]pyrimidines as synthons for the preparation of polycondensed heterocycles: reaction with α-bromoketones-Reference-Cited by-同舟云学术

Partially hydrogenated 2-amino[1,2,4]triazolo[1,5-a]pyrimidines as synthons for the preparation of polycondensed heterocycles: reaction with α-bromoketones

Published:2015-09 Issue:36 Volume:71 Page:6259-6271
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Chernyshev Victor M.^ORCID,Pyatakov Dmitry A.,Astakhov Alexander V.,Sokolov Andrey N.,Fakhrutdinov Artem N.,Rybakov Victor B.,Chernyshev Vladimir V.

Funder

Russian Science Foundation

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference67 articles.

1. Recent Progress in 1,2,4-Triazolo[1,5-a]pyrimidine Chemistry

2. Nafion-H® catalyzed efficient one-pot synthesis of triazolo[5,1-b]quinazolinones and triazolo[1,5-a]pyrimidines: A green strategy

3. One-Pot Synthesis of 5-Unsubstituted-6-Aroyl[1,2,4]triazolo[1,5-a]pyrimidine Utilizing Biginelli-Like Multicomponent Reaction of Enaminones with 3-Amino-1,2,4- triazole as the Urea Component

4. Multicomponent reactions for synthesis of bioactive polyheterocyclic ring systems under controlled microwave irradiation

5. Ultrasound irradiation promotes the synthesis of new 1,2,4-triazolo[1,5-a]pyrimidine

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