Asymmetric Hydrogenation of Dehydrodipeptides with Rhodium (I)–Chiral Diphosphinites. Selective (S, S)-and (R, R)-Product Formation by Double Asymmetric …

M Yatagai, T Yamagishi, M Hida

Index: Yatagai; Yamagishi; Hida Bulletin of the Chemical Society of Japan, 1984 , vol. 57, # 3 p. 823 - 826

Full Text: HTML

Citation Number: 18

Abstract

In the hydrogenation of dehydrodipeptides, the effect of chiral center of the substrate ((S) or (R)) on the asymmetric induction was examined using the catalysts of Rh (I)–chiral diphosphinite containing pyrrolidine moiety (POP). The catalysts with POP's having the ω- (dimethylamino) alkyl group indicated an extremely large double asymmetric induction to give (S, S)-or (R, R)-product in high stereoselectivities, depending on the chiral center of ...

Related Articles:

Effects of solvent and temperature on the 1, 4-asymmetric induction in the diastereoselective hydrogenation of dehydrodipeptides

[Ikeda; Yamagishi; Yamaguchi; Hida Bulletin of the Chemical Society of Japan, 1989 , vol. 62, # 11 p. 3508 - 3512]

Effective asymmetric hydrogenation of dehydrodipeptides with rhodium (I)-new chiral diphosphinite systems

[Yatagai, Masanobu; Zama, Masanobu; Yamagishi, Takamichi; Hida, Mitsuhiko Chemistry Letters, 1983 , p. 1203 - 1206]

Development and biological applications of quantum mechanical continuum solvation models

[Smith; Spackman Journal of Biological Chemistry, 1955 , vol. 212, p. 271,291]

Se-(9-Fluorenylmethyl) selenoesters; preparation, reactivity, and use as convenient synthons for selenoacids

[Chen, Wenteng; Shao, Jiaan; Hu, Miao; Yu, Wanwan; Giulianotti, Marc A.; Houghten, Richard A.; Yu, Yongping Chemical Science, 2013 , vol. 4, # 3 p. 970 - 976]

Development and biological applications of quantum mechanical continuum solvation models

[Smith; Spackman Journal of Biological Chemistry, 1955 , vol. 212, p. 271,291]

More Articles...