Preparation of Acidic 5-Hydroxy-1,2,3-triazoles via the Cycloaddition of Aryl Azides with β-Ketoesters-Reference-Cited by-同舟云学术

Preparation of Acidic 5-Hydroxy-1,2,3-triazoles via the Cycloaddition of Aryl Azides with β-Ketoesters

Published:2021-07-27 Issue:17 Volume:86 Page:11354-11360
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Pacifico Roberta¹,Destro Dario¹,Gillick-Healy Malachi W.¹²,Kelly Brian G.²,Adamo Mauro F. A.¹^ORCID

Affiliation:

1. Centre for Synthesis and Chemical Biology (CSCB), Department of Chemistry, Royal College of Surgeons in Ireland, 123 St. Stephen’s Green, Dublin 2, Ireland

2. KelAda Pharmachem Ltd., A1.01 Science Centre South, Belfield, Dublin 4, Ireland

Funder

Irish Research Council

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c00778

Reference30 articles.

1. Medicinal attributes of 1,2,3-triazoles: Current developments

2. 1,2,3,-Triazole-Based Catalysts: From Metal- to Supramolecular Organic Catalysis

3. Applications of Metal-Free 1,2,4-Triazole Derivatives in Materials Science

4. A Strain-Promoted [3 + 2] Azide−Alkyne Cycloaddition for Covalent Modification of Biomolecules in Living Systems

5. Evaluation of 1,2,3‐Triazoles as Amide Bioisosteres In Cystic Fibrosis Transmembrane Conductance Regulator Modulators VX‐770 and VX‐809

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