Journal
ORGANIC LETTERS
Volume 18, Issue 22, Pages 5916-5919Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b03019
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Funding
- US National Science Foundation [CHE-1265488]
- Graduate College, University of Iowa
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [1265488] Funding Source: National Science Foundation
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Alkylidene dihydropyridines (anhydrobases) prepared via dearomatization of N-acylated 4-(aminomethyl)pyridines participate in [3 + 2] cyclocondensation reactions with aryldiazonium cations to afford substituted 1,2,4-triazolium salts or neutral 1,2,4-triazoles in high isolated yield. The reaction proceeds in the presence of a variety of N-acyl groups and aryl-susbtituted diazonium salts and offers a general route to pyridyl-substituted 1,2,4-triazoles.
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