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Interrupted CuAAC‐Thiolation for the Construction of 1,2,3‐Triazole‐Fused Eight‐Membered Heterocycles from <i>O</i>‐/<i>N</i>‐Propargyl derived Benzyl Thiosulfonates with Organic Azides

Raju Jannapu Reddy, Md. Waheed, Arram Haritha Kumari, Gamidi Rama Krishna

2021Advanced Synthesis & Catalysis28 citationsDOI

Abstract

Abstract A copper(I)‐catalyzed interrupted click‐sulfenylation of O‐/N ‐propargyl benzyl thiosulfonates with organic azides has been disclosed. The unified CuAAC‐thiolation provides a wide range of triazole‐fused eight‐membered heterocycles in good to high (51–94%) yields under mild reaction conditions. Moreover, a three‐component reaction is also achieved involving O‐/N ‐propargyl benzyl thiosulfonates, benzyl bromide, and sodium azide to deliver fused‐triazoles in 61–74% yields. From a synthetic point of view, the present protocol has been demonstrated at gram‐scale reactions. A plausible mechanism is also proposed based on experimental results and control experiments. magnified image

Topics & Concepts

ChemistryPropargylClick chemistrySodium azideCombinatorial chemistryPropargyl bromideTriazoleAzideBenzyl bromide1,2,3-TriazoleCatalysisOrganic chemistrySulfur-Based Synthesis TechniquesClick Chemistry and ApplicationsCyclopropane Reaction Mechanisms
Interrupted CuAAC‐Thiolation for the Construction of 1,2,3‐Triazole‐Fused Eight‐Membered Heterocycles from <i>O</i>‐/<i>N</i>‐Propargyl derived Benzyl Thiosulfonates with Organic Azides | Litcius