84127-05-9Relevant articles and documents
DESIGN OF METHOXY-SUBSTITUED BPPM ANALOGUES AND THEIR APPLICATION TO THE ASYMMETRIC SYNTHESIS OF N-ACETYLPHENYLALANINE
Takahashi, Hisashi,Achiwa, Kazuo
, p. 3230 - 3233 (2007/10/02)
We described the preparation of methoxy-substitued BPPM ((2S,4S)-N-(tert-butoxycarbonyl)-4-(diphenylphosphino)-2-pyrrolidine) analogues for highly effective asymmetric hydrogenation of (Z)-acetamidocinnamic acid. o-Methoxy-BPPM-Rh+ was very high optical yield (98percent enantiomeric excess (ee), (R)) and p-methoxy-BPPM-Rh+ was very actively catalytic (/=104).On the bases of these result and our respectively control concept, we developed a highly effective chiral ligand (5) for asymmetric synthesis of N-acetylphenylalanine.