Enantioselective synthesis of (R)-tolterodine via CuH-catalyzed asymmetric conjugate reduction
(Chemical Equation Presented) An efficient and highly enantioselective method for the preparation of (R)-tolterodine is described. The synthesis was performed by CuH-catalyzed asymmetric conjugate reduction of a β,β-diaryl-substituted unsaturated nitrile
Yoo, Kihyun,Kim, Hyohyun,Yun, Jaesook
supporting information; experimental part
p. 4232 - 4235
(2009/09/25)
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