Cu/chiral phosphoric acid-catalyzed radical-initiated asymmetric aminosilylation of alkene with hydrosilane
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摘要:
The catalytic radical-initiated asymmetric 1,2-aminosilylation of alkene with a hydrosilane under Cu(Ⅰ)/CPA cooperative catalysis has been developed.This method features the use of hydrosilane as the reductive radical precursor,enabling efficient access to skeletally diverse silicon-containing azaheterocycles including pyrrolidine,indoline and isoindoline bearing an α-tertiary stereocenter with high enantioselectivity.The key to the success includes the use of Cu(Ⅰ)/CPA cooperative catalyst system and the β-silicon effect of the silyl group to stabilize the in situ generated carbocation intermediate.