An efficient and metal-free synthetic protocol for mono-, bis-, and spiro[1,2,4]triazolo[1,5-a]pyridines utilizing 1,2-diaminopyridine derivative via C–N bond formation-Reference-Cited by-同舟云学术

An efficient and metal-free synthetic protocol for mono-, bis-, and spiro[1,2,4]triazolo[1,5-a]pyridines utilizing 1,2-diaminopyridine derivative via C–N bond formation

Published:2021-08-06 Issue:20 Volume:51 Page:3116-3124
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

El-Sayed Hassan A.¹^ORCID,Said Said A.¹,Abd El-Hamid Ahmed M.¹

Affiliation:

1. Department of Chemistry, Faculty of Science, Zagazig University, Zagazig, Egypt

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2021.1961276

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3. Novel 1,2,4-Triazolo[1,5-a]pyridines and Their Fused Ring Systems Attenuate Oxidative Stress and Prolong Lifespan of Caenorhabiditis elegans

4. Hamdouchi, C.; Maiti, P. Phenyl-triazolo-pyridine compounds, WO 2015105786A1, 2015.

5. (2S,3S)-3-Amino-4-(3,3-difluoropyrrolidin-1-yl)-N,N-dimethyl-4-oxo-2-(4-[1,2,4]triazolo[1,5-a]- pyridin-6-ylphenyl)butanamide: A Selective α-Amino Amide Dipeptidyl Peptidase IV Inhibitor for the Treatment of Type 2 Diabetes

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