Hypervalent iodine (III) compounds have found wide application in modern organic
chemistry as environmentally friendly reagents and catalysts. Hypervalent iodine reagents …

An important strategy for the efficient generation of diversity in molecular structures is the
utilization of common starting materials in chemodivergent transformations. The most …

In this paper, we report an efficient one-pot three-component reaction sequences comprising
Cu (I)-catalyzed 1, 3-dipolar cycloaddition (CuAAC) followed by Cu-catalyzed arylation of …

Vinyl sulfones are privileged motifs for assembling prevalent biologically active molecules
and represent “gateway functional groups” in medicinal chemistry and drug discovery …

1-Iodoalkynes and 1, 3-diynes are versatile chemical intermediates and pharmaceutically
valuable ingredients. In this study, copper mediated on-DNA alkyne iodination and Cadiot …

We describe a catalyst-free 1, 2-trans-dihalogenation of alkynes with an unprecedented
substrate scope and exclusive regio-and stereoselectivity. This versatile dihalogenation …

This study presents an efficient strategy for constructing 3H-1, 2, 4-triazol-3-ones via a
copper-promoted [3+ 2] annulation reaction of amidine hydrochlorides and isocyanates. This …

We report the synthesis of 1, 4-diaryl-5-cyano-1, 2, 3-triazoles from azides and alkynes via
two copper-mediated steps. Aryl-substituted cyanotriazoles are emissive in nonpolar …

A visible light-induced vicinal diazidation of various alkenes using stable sulfonium bis
(acetoxy) iodate (I) and sodium azide as a radical precursor is described. The …

Highly enantioselective C2 alkylation and inverse-electron-demand [3+ 2]-cycloaddition of 3-
methylindoles with 2, 2′-diester aziridine were accomplished. The chemodivergent …