Enzymatic hydrolysis of (±)-trans-1, 2-diacetozycycloalkanes. A facile route to optically-active cycloalkane-1, 2-diols
…, VSB Gaudet, K Laumen, MP Schneider
Index: Crout, David H. G.; Gaudet, Veronique S. B.; Laumen, Kurt; Schneider, Manfred P. Journal of the Chemical Society, Chemical Communications, 1986 , # 10 p. 808 - 810
Full Text: HTML
Citation Number: 34
Abstract
Hydrolytic enzymes are well known for their capability of enantiomer differentiation.1 While optically-active carboxylic acids have been obtained frequently by enantioselective hydrolysis of racemic (or prochiral) esters,2 the corresponding preparation of alcohols (or 1,2-diols) has received much less attention in the past.3 In this communication we report the ... Published on 01 January 1986. Downloaded by google on 17/02/2016 13:24:18.
Related Articles:
[Cunningham, Allan F.; Kuendig, E. Peter Journal of Organic Chemistry, 1988 , vol. 53, # 8 p. 1823 - 1825]
[Mueller, Christian E.; Wanka, Lukas; Jewell, Kevin; Schreiner, Peter R. Angewandte Chemie - International Edition, 2008 , vol. 47, # 33 p. 6180 - 6183]
[Hrdina, Radim; Mueller, Christian E.; Schreiner, Peter R. Chemical Communications, 2010 , vol. 46, # 15 p. 2689 - 2690]
[Zheng, Huabao; Reetz, Manfred T. Journal of the American Chemical Society, 2010 , vol. 132, # 44 p. 15744 - 15751]
[Tang; Kennedy Tetrahedron Letters, 1992 , vol. 33, # 51 p. 7823 - 7826]