1-Protected 5-amido 1,2,3-triazoles via ruthenium-catalyzed [3+2] cycloaddition of azides and ynamides-Reference-Cited by-同舟云学术

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1-Protected 5-amido 1,2,3-triazoles via ruthenium-catalyzed [3+2] cycloaddition of azides and ynamides

Published:2007-08 Issue:34 Volume:63 Page:8094-8098
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Oppilliart Sophie,Mousseau Guillaume,Zhang Li,Jia Guochen,Thuéry Pierre,Rousseau Bernard,Cintrat Jean-Christophe

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference54 articles.

1. Organic Azides: An Exploding Diversity of a Unique Class of Compounds

2. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides

3. 1,3-Dipolar Cycloadditions. Past and Future

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1. Modular Synthesis of Tripeptide Analogs with an Aminobitriazole Skeleton Using Diynyl Benziodoxolone as a Trivalent Platform;The Journal of Organic Chemistry;2024-07-31

2. Recent Developments in the Ruthenium‐Catalyzed Azide Alkyne Cycloaddition (RuAAC) Reaction;European Journal of Organic Chemistry;2024-06-18

3. RuAAC ‘Click Chemistry’-Mediated Synthesis of 1,5-Disubstituted 1,2,3-Triazoles;Materials Horizons: From Nature to Nanomaterials;2024

4. Base-Promoted [3+2] Annulation of Carbodiimides with Diazoacetonitrile for Synthesis of 5-Amino-4-cyano-1,2,3-triazoles;Synlett;2023-11-22

5. Recent Progress on Synthesis of Functionalized 1,5-Disubstituted Triazoles;Current Organic Synthesis;2023-04-18

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