Tetrahedron: Asymmetry

Enzyme assisted preparation of enantiomerically pure β-adrenergic blockers II. Building blocks of high optical purity and their synthetic conversion

U Ader, MP Schneider

Index: Ader, Ulrich; Schneider, Manfred P. Tetrahedron: Asymmetry, 1992 , vol. 3, # 2 p. 205 - 208

Full Text: HTML

Citation Number: 42

Abstract

Abstract Based on previous screening results a series of potential building blocks t2–4 for β- adrenergic blockers were prepared both by enzymatic hydrolysis and acyltransfer and further transformed into the corresponding oxiranes and aminoalcohols of defined absolute configurations.

Related Articles:

Determination of the enantiomeric purity and the configuration of β-aminoalcohols using (R)-2-fluorophenylacetic acid (AFPA) and fluorine-19 NMR: application to β- …

[Apparu, Marcel; Ben Tiba, Younes; Leo, Pierre-Marc; Hamman, Sylvain; Coulombeau, Christian Tetrahedron Asymmetry, 2000 , vol. 11, # 14 p. 2885 - 2898]

Enantioselective ring opening of epoxides with trimethylsilyl azide (TMSN 3) in the presence of β-cyclodextrin: an efficient route to 1, 2-azido alcohols

[Kamal, Ahmed; Arifuddin; Rao, Maddamsetty V. Tetrahedron Asymmetry, 1999 , vol. 10, # 22 p. 4261 - 4264]

Stereoselective synthesis of (S)-propanol amines: lipase catalyzed opening of epoxides with 2-propylamine

[Kamal, Ahmed; Damayanthi, Yalamati; Rao, Maddamsetty V. Tetrahedron: Asymmetry, 1992 , vol. 3, # 11 p. 1361 - 1364]

More Articles...