![Synthesis and characterization of Triazolo[4,3-c]pyrimidine library - Vilapara, Kalpesh;Gami, Sagar](https://bilder.buecher.de/produkte/57/57553/57553514z.jpg "Synthesis and characterization of Triazolo[4,3-c]pyrimidine library - Vilapara, Kalpesh;Gami, Sagar")
Andere Kunden interessierten sich auch für
![Progress in Heterocyclic Chemistry]( "Progress in Heterocyclic Chemistry")
Progress in Heterocyclic Chemistry152,99 €![Development of Chemistry-Based Screening Platform for Access to Mirror-Image Library of Natural Products]( "Development of Chemistry-Based Screening Platform for Access to Mirror-Image Library of Natural Products")
Development of Chemistry-Based Screening Platform for Access to Mirror-Image Library of Natural Products76,99 €![Synthesis and Characterization of Bi12SiO20 Thin Films]( "Synthesis and Characterization of Bi12SiO20 Thin Films")
Synthesis and Characterization of Bi12SiO20 Thin Films39,99 €![Synthesis And Characterization Of Biobased Polymer Composites]( "Synthesis And Characterization Of Biobased Polymer Composites")
Synthesis And Characterization Of Biobased Polymer Composites32,99 €![Synthesis and characterization of Transition Metal Complexes]( "Synthesis and characterization of Transition Metal Complexes")
Synthesis and characterization of Transition Metal Complexes39,99 €![Zeolites for Pharmaceutically Important Drug Synthesis]( "Zeolites for Pharmaceutically Important Drug Synthesis")
Zeolites for Pharmaceutically Important Drug Synthesis51,99 €![Synthesis and Spectral Characterization of Novel Organic Compounds]( "Synthesis and Spectral Characterization of Novel Organic Compounds")
Synthesis and Spectral Characterization of Novel Organic Compounds51,99 €
A novel [1,2,4]triazolo[4,3-c]pyrimidine-8-carboxamide libraries were synthesized via oxidative cyclization of hydrazono-1,6-dihydropyrimidine-5-carboxamide intermediates by the application of Iodobenzenediacetate as a sole cyclizating agent. Here, we report one pot sequential strategy to generate corresponding triazolopyrimidines by condensation of preprepared -acylketene dithioacetals and arylamidines. Moreover, this process describes the application of presynthesized arylamidines which omits the transition metal catalyzed Suzuki-Miyaura cross coupling reaction hence signify the atom- and step-economic methodology.