Tetrahedron: Asymmetry

Deracemization of (±)-mandelic acid using a lipase–mandelate racemase two-enzyme system

UT Strauss, K Faber

Index: Tetrahedron Asymmetry, , vol. 10, # 21 p. 4079 - 4081

Full Text: HTML

Citation Number: 78

Abstract

... Please enable JavaScript to use all the features on this page. Tetrahedron: Asymmetry. Volume 10, Issue 21, 29 October 1999, Pages 4079–4081. Cover image Cover image. ... References. 1; Strauss, UT; Felfer, U.; Faber, K. Tetrahedron: Asymmetry1999, 10, 107–110. ...

Related Articles:

Controlled racemization and asymmetric transformation of α-substituted carboxylic acids in the melt

[Tetrahedron Asymmetry, , vol. 10, # 19 p. 3701 - 3718]

Optically active α??acetoxycarboxylic acids and α??hydroxycarboxylic acids by enzyme??aided syntheses

[Journal fuer Praktische Chemie/Chemiker-Zeitung, , vol. 334, # 6 p. 526 - 528]

Highly stereoselective Friedel–Crafts type cyclization. Facile access to enantiopure 1, 4-dihydro-4-phenyl isoquinolinones

[Tetrahedron, , vol. 59, # 40 p. 8049 - 8056]

Investigations into the parallel kinetic resolution of acetyl mandelic acid

[Tetrahedron Letters, , vol. 49, # 52 p. 7398 - 7402]

Development of new HPLC chiral stationary phases based on native and derivatized cyclofructans

[Analytical Chemistry, , vol. 81, # 24 p. 10215 - 10226]

More Articles...