Waser, JeromeNambu, HisanoriCarreira, Erick M.2007-12-172007-12-172007-12-17200510.1021/ja052164rhttps://infoscience.epfl.ch/handle/20.500.14299/15789Conversion 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, tetramethyldisiloxane). [on SciFinder (R)]Alkenes Role: RCT (Reactant)RACT (Reactant or reagent) (prepn. of alkyl azides via cobalt-catalyzed hydroazidation of olefins); Azides Role: SPN (Synthetic preparation)PREP (Preparation) (prepn. of alkyl azides via cobalt-catalyzed hydroazidation of olefins)alkyl azide prepn cobalt catalysis hydroazidation olefintext::journal::journal article::research article