A stereoselective and convenient route has been demonstrated to access ()-1,2-diazido alkenes from the corresponding 1,2-diboronic esters a copper-mediated reaction with sodium azide. Alternately, mono-functionalization was regioselectively carried out with trimethylsilyl azide as an azidation reactant. The conversion of bis-azides to the corresponding bis-triazoles can be readily achieved in the presence of copper sulfate and sodium ascorbate, while the modification of the catalytic system opened a new convenient route to bis-triazolo-pyrazines, a new class of fused heterocycles.

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http://dx.doi.org/10.1021/acs.joc.0c01980DOI Listing

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