Enantioselective Rh-catalyzed hydrogenation of enol acetates and enol carbamates with monodentate phosphoramidites
L Panella, BL Feringa, JG de Vries, AJ Minnaard
Index: Panella, Lavinia; Feringa, Ben L.; De Vries, Johannes G.; Minnaard, Adriaan J. Organic Letters, 2005 , vol. 7, # 19 p. 4177 - 4180
Full Text: HTML
Citation Number: 63
Abstract
Monodentate phosphoramidites, in particular PipPhos and its octahydro analogue, are excellent ligands for the rhodium-catalyzed asymmetric hydrogenation of aromatic enol acetates, enol carbamates, and 2-dienol carbamates up to 98% ee. These latter substrates were hydrogenated selectively to the carbamates of the allyl alcohol.
Related Articles:
[Mahe, Roger; Sasaki, Yoshiyuki; Bruneau, Christian; Dixneuf, Pierre H. Journal of Organic Chemistry, 1989 , vol. 54, # 7 p. 1518 - 1523]
[Sengupta, Saumitra; Snieckus, Victor Journal of Organic Chemistry, 1990 , vol. 55, # 22 p. 5680 - 5683]
[Sasaki, Yoshiyuki; Dixneuf, Pierre H. Journal of Organic Chemistry, 1987 , vol. 52, # 2 p. 314 - 315]
[Overberger,C.G. et al. Journal of Organic Chemistry, 1962 , vol. 27, p. 4331 - 4337]
[Sengupta, Saumitra; Snieckus, Victor Journal of Organic Chemistry, 1990 , vol. 55, # 22 p. 5680 - 5683]