Diastereoselective Synthesis of the Hydroxyethylene Dipeptide Isostere of Leu–Val

Autor: Nishi, Takahide, Kataoka, Mitsuru, Morisawa, Yasuhiro
Zdroj: Chemistry Letters; November 1989, Vol. 18 Issue: 11 p1993-1996, 4p
Abstrakt: The synthesis of hydroxyethylene dipeptide isostere of Leu–Val, a transition-state mimic, is described. The key steps of this synthetic approach are the homogeneous asymmetric hydrogenation of γ-keto esters by BINAP–Ru(II) complex, and the construction of a 2(S)-isopropyl unit.
Databáze: Supplemental Index