Facile Regioselective Green Synthesis of Triazolo [4,3-a] Pyrimidines in Aqueous Medium
Authors: Dandia, Anshu; Singh, Ruby; Singh, Dharmendra; Arya, Kapil
Source: Letters in Organic Chemistry, Volume 6, Number 1, January 2009 , pp. 100-105(6)
Publisher: Bentham Science Publishers
Abstract:
Regioselectivity is investigated in multi-component reaction of amino triazole, carbonyl compounds and α- cyano esters derivative and exclusive synthesis of triazolopyrimidines is developed in aqueous medium in excellent yields in shorter period using microwaves or ultrasonic waves. Path and mechanism of the reaction has also been discussed. The operational simplicity, environmental friendly conditions, regioselective formation of target product, high yield in significantly very short reaction time, are major benefits.Keywords: α-Cyano acrylates; microwave irradiations; ultrasound; aqueous medium; triazolopyrimidines
Document Type: Research article
DOI: http://dx.doi.org/10.2174/157017809787003124
Publication date: 2009-01-01
- Letters in Organic Chemistry publishes original letters on all areas of organic chemistry including synthesis, bioorganic, medicinal, natural products, organometallic, supramolecular, molecular recognition and physical organic chemistry. The emphasis is placed on publishing quality papers very rapidly. Letters are processed rapidly and take full advantage of the Internet technology both for the submission and the review of the manuscripts.
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- By this author: Dandia, Anshu ; Singh, Ruby ; Singh, Dharmendra ; Arya, Kapil

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