Qian, DeyunHu, Xile2019-11-272019-11-272019-11-272019-11-1410.1002/anie.201912629https://infoscience.epfl.ch/handle/20.500.14299/163389WOS:000496280900001Nickel hydride (NiH) catalyzed hydrocarbonation has emerged as an efficient approach to construct new C-C bonds containing at least one C(sp(3)) center. However, the regioselectivity of this reaction is by far dictated by substrates. Described here is a strategy to achieve two different regioselectivites of hydroalkylation of the same substrates by using ligand control. This strategy enables the first regiodivergent hydroalkylation of 3-pyrrolines, yielding both 2- and 3-alkylated pyrrolidines, valuable synthetic intermediates and common motifs in many bioactive molecules. This method demonstrates broad scope and high functional-group tolerance, and can be applied in late-stage functionalizations.Chemistry, MultidisciplinaryChemistryalkenesheterocycleshydroalkylationnickelreaction mechanismsmedicinal chemists toolboxcarboxylic-acidshydroarylationremotealkenesfunctionalizationolefinsindolizidinehydrocarbonsbromidestext::journal::journal article::research article