Chemo-enzymatic synthesis of 1,2- and 1,3- amino-alcohols and their use in the enantioselective reduction of acetophenone and anti-acetophenone oxime methyl ether with borane.
暂无分享,去创建一个
[1] R. W. Emblidge,et al. A simple conversion of diethyl phenylmalonate with metal hydride to the corresponding primary diol: a competing reaction between reduction and metallation , 1989 .
[2] E. Corey,et al. A new chiral catalyst for the enantioselective synthesis of secondary alcohols and deuterated primary alcohols by carbonyl reduction , 1989 .
[3] Yoji Sakito,et al. Asymmetric reduction of oxime ethers. Distinction of anti and syn isomers leading to enantiomeric amines. , 1988 .
[4] B. Feringa,et al. Synthesis of arylimines from N-silylamides and aryllithium compounds , 1986 .
[5] T. Furuta,et al. Photochemical rearrangement approach to the total synthesis of (±)-pinguisone and (±)-deoxopinguisone , 1985 .
[6] A. Hercouet,et al. Versatilite de reactivite de l`acetylene dicarbaldehyde et des aldehydes α-acetyleniques a l'egard des dienes conjugues cycliques et heterocycliques en milieu acide , 1981 .
[7] K. Ninomiya,et al. Diphenylphosphoryl azide. A new convenient reagent for a modified Curtus reaction and for the peptide synthesis. , 1972, Journal of the American Chemical Society.
[8] G. Bernáth,et al. Stereochemical studies—XIII: Cyclic aminoalcohols and related compounds—VI synthesis of the four 2-amino-4-t-butylcyclopentanol isomers , 1972 .