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Azides are building blocks of increasing importance in synthetic chemistry, chemical biology, and materials science. Azidobenziodoxolone (ABX, Zhdankin reagent) is a valuable azide source, but its safety profile has not been thoroughly established. Herein, ...
Conversion of unactivated olefins to azides was achieved with high Markovnikov selectivity for a broad range of alkenes by using 6 mol % Co(BF4).6H2O and ligand I, with 3 equiv of tosyl azide as the nitrogen source and simple silanes (e.g., PhSiH3, tetrame ...
2,3-Dichloropyridines undergo a mono- or a dicarbonylation in the presence of carbon monoxide, an alc., and a palladium catalyst, affording selectively either alkyl 3-chloropyridine-2-carboxylates or dialkyl pyridine-2,3-dicarboxylates in good yields, depe ...
Treatment of olefins with an excess of di-tert-Bu azodicarboxylate, an equimolar amt. of PhSiH3, and a catalytic amt. of a Co(III) catalyst afforded the Markovnikov hydrazide products, e.g., I, for a broad range of olefins, in good yields. [on SciFinder (R ...
Enhanced activity, lower catalyst loading, shorter reaction time, and expanded substrate scope are the advantages of [Mn(dpm)3] over Co catalysts in the hydrohydrazination reaction of alkenes. Thus, sterically hindered alkenes, including tetrasubstituted a ...
