122292-74-4Relevant academic research and scientific papers
EFFICIENT PREPARATION OF NEW CHIRAL SYNTHONS USEFUL FOR (+)-CARBACYCLIN SYNTHESIS BY UTILIZING ENZYMATIC HYDROLYSIS OF PROCHIRAL ?-SYMMETRIC DIESTERS
Nagao, Yoshimitsu,Kume, Masaharu,Wakabayashi, Robin Chikako,Nakamura, Takeshi,Ochiai, Masahito
, p. 239 - 242 (2007/10/02)
Enzymatic hydrolyses of some prochiral ?-symmetric dimethyl esters employing porcine liver esterase and porcine pancreatic lipase were investigated, resulting in the enantioselective preparation of the corresponding new monoesters useful for (+)-carbacycl
Enzyme-Catalyzed Asymmetric Synthesis. 8. Enantioselectivity of Pig Liver Esterase Catalyzed Hydrolyses of 4-Substituted Meso Cyclopentane 1,2-Diesters
Gais, Hans-Joachim,Buelow, Gerd,Zatorski, Andrzej,Jentsch, Mathias,Maidonis, Peter,Hemmerle, Horst
, p. 5115 - 5122 (2007/10/02)
Hydrolyses of meso-1,2-cyclopentanedicarboxylic acid bis(methyl esters) bearing in the 4-position an oxo, methylene, cis-hydroxy, trans-hydroxy,cis-acetoxy, trans-acetoxy, cis-methoxy, cis-tert-butoxy, ethylenedioxy, propylenedioxy, dimethyl propylenediox
