Enamine/Enolate-Mediated Organocatalytic Azide-Carbonyl [3+2] Cycloaddition Reactions for the Synthesis of Densely Functionalized 1,2,3-Triazoles

An Organocatalytic Azide-Aldehyde [3+2] Cycloaddition: High-Yielding Regioselective Synthesis of 1,4-Disubstituted 1,2,3-Triazoles

(2014) Dhevalapally B. Ramachary et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

A Metal-Free Three-Component Reaction for the Regioselective Synthesis of 1,4,5-Trisubstituted 1,2,3-Triazoles

(2014) Joice Thomas et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

An efficient one-pot strategy for the highly regioselective metal-free synthesis of 1,4-disubstituted-1,2,3-triazoles

(2014) Akbar Ali et al.   CHEMICAL COMMUNICATIONS

1,2,3-Triazole in Heterocyclic Compounds, Endowed with Biological Activity, through 1,3-Dipolar Cycloadditions

(2014) Antonino Lauria et al.   EUROPEAN JOURNAL OF ORGANIC CHEMISTRY

Direct access to 1,2,3-triazoles through organocatalytic 1,3-dipolar cycloaddition reaction of allyl ketones with azides

(2014) Wenjun Li et al.   GREEN CHEMISTRY

I2/TBPB Mediated Oxidative Reaction of N-Tosylhydrazones with Anilines: Practical Construction of 1,4-Disubstituted 1,2,3-Triazoles under Metal-Free and Azide-Free Conditions

(2014) Zhong-Jian Cai et al.   ORGANIC LETTERS

A Metal-Free Multicomponent Cascade Reaction for the Regiospecific Synthesis of 1,5-Disubstituted 1,2,3-Triazoles

(2013) Guolin Cheng et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Direct access to triazole-olefins through catalytic cycloaddition of azides to unsaturated aldehydes

(2013) Wenjun Li et al.   CHEMICAL COMMUNICATIONS

Click Chemistry for Drug Development and Diverse Chemical–Biology Applications

(2013) Prakasam Thirumurugan et al.   CHEMICAL REVIEWS

Organocatalytic Triazole Formation, Followed by Oxidative Aromatization: Regioselective Metal-Free Synthesis of Benzotriazoles

(2013) Dhevalapally B. Ramachary et al.   CHEMISTRY-A EUROPEAN JOURNAL

Organocatalytic 1,3-dipolar cycloaddition reactions of ketones and azides with water as a solvent

(2013) Dwun Kit Jonathan Yeung et al.   GREEN CHEMISTRY

Traceless Tosylhydrazone-Based Triazole Formation: A Metal-Free Alternative to Strain-Promoted Azide-Alkyne Cycloaddition

(2012) Sander S. van Berkel et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Amine-Catalyzed [3+2] Huisgen Cycloaddition Strategy for the Efficient Assembly of Highly Substituted 1,2,3-Triazoles

(2012) Lei Wang et al.   CHEMISTRY-A EUROPEAN JOURNAL

Moderating Strain without Sacrificing Reactivity: Design of Fast and Tunable Noncatalyzed Alkyne–Azide Cycloadditions via Stereoelectronically Controlled Transition State Stabilization

(2012) Brian Gold et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Synthesis of arylselanyl-1H-1,2,3-triazole-4-carboxylates by organocatalytic cycloaddition of azidophenyl arylselenides with β-keto-esters

(2012) Natália Seus et al.   TETRAHEDRON

Click Chemistry Finds Its Way into Covalent Porous Organic Materials

(2011) Thierry Muller et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Organocatalytic Synthesis of 1,2,3-Triazoles from Unactivated Ketones and Arylazides

(2011) Mokhtaria Belkheira et al.   CHEMISTRY-A EUROPEAN JOURNAL

Organocatalytic Enamide-Azide Cycloaddition Reactions: Regiospecific Synthesis of 1,4,5-Trisubstituted-1,2,3-Triazoles

(2011) Lee Jin Tu Danence et al.   CHEMISTRY-A EUROPEAN JOURNAL

Click Chemistry: 1,2,3-Triazoles as Pharmacophores

(2011) Sandip G. Agalave et al.   Chemistry-An Asian Journal

New Lead Structures in Antifungal Drug Discovery

(2011) Chunquan Sheng et al.   CURRENT MEDICINAL CHEMISTRY

Cu-free click cycloaddition reactions in chemical biology

(2010) John C. Jewett et al.   CHEMICAL SOCIETY REVIEWS

Amino Acid-Catalyzed Cascade [3+2]-Cycloaddition/Hydrolysis Reactions Based on the Push-Pull Dienamine Platform: Synthesis of Highly FunctionalizedNH-1,2,3-Triazoles

(2008) Dhevalapally B. Ramachary et al.   CHEMISTRY-A EUROPEAN JOURNAL

Theory of 1,3-Dipolar Cycloadditions: Distortion/Interaction and Frontier Molecular Orbital Models

(2008) Daniel H. Ess et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY