Direct extraction of phenylacetic acid from immobilised enzymatic hydrolysis of penicillin G with cloud point extraction

2006 ◽  
Vol 81 (4) ◽  
pp. 560-565 ◽  
Author(s):  
Zhilong Wang ◽  
Yajing Guo ◽  
Da Bao ◽  
Hanshi Qi
2008 ◽  
Vol 136 ◽  
pp. S391
Author(s):  
Mai Ngoc Lan ◽  
Sung Ho Ha ◽  
Yoon-Mo Koo

2003 ◽  
Vol 19 (6) ◽  
pp. 1639-1642 ◽  
Author(s):  
O. Abian ◽  
C. Mateo ◽  
G. Fernandez-Lorente ◽  
J.M. Guisan ◽  
R. Fernandez-Lafuente

Catalysts ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 113 ◽  
Author(s):  
Andrea Pinto ◽  
Immacolata Serra ◽  
Diego Romano ◽  
Martina Contente ◽  
Francesco Molinari ◽  
...  

Preparation of optically-pure derivatives of 2-hydroxy-2-(3-hydroxyphenyl)-2-phenylacetic acid of general structure 2 was accomplished by enzymatic hydrolysis of the correspondent esters. A screening with commercial hydrolases using the methyl ester of 2-hydroxy-2-(3-hydroxyphenyl)-2-phenylacetic acid (1a) showed that crude pig liver esterase (PLE) was the only preparation with catalytic activity. Low enantioselectivity was observed with substrates 1a–d, whereas PLE-catalysed hydrolysis of 1e proceeded with good enantioselectivity (E = 28), after optimization. Enhancement of the enantioselectivity was obtained by chemical re-esterification of enantiomerically enriched 2e, followed by sequential enzymatic hydrolysis with PLE. The preparation of optically-pure (S)-2e was validated on multi-milligram scale.


1996 ◽  
Vol 208 (1) ◽  
pp. 133-144 ◽  
Author(s):  
I. Miesiąc ◽  
K. Schügerl ◽  
A. Hasler ◽  
J. Szymanowski

2002 ◽  
Vol 78 (4) ◽  
pp. 395-402 ◽  
Author(s):  
M. B. Diender ◽  
A. J. J. Straathof ◽  
T. van der Does ◽  
C. Ras ◽  
J. J. Heijnen

Sign in / Sign up

Export Citation Format

Share Document