Microbial production of optically active β-phenylalanine ethyl ester through stereoselective hydrolysis of racemic β-phenylalanine ethyl ester

2006 ◽  
Vol 70 (6) ◽  
pp. 663-669 ◽  
Author(s):  
Jun Ogawa ◽  
Junichi Mano ◽  
Sakayu Shimizu
1980 ◽  
Vol 18 (10) ◽  
pp. 647-651 ◽  
Author(s):  
Mamoru Nango ◽  
Hiroshi Kozuka ◽  
Yoshiharu Kimura ◽  
Nobuhiko Kuroki ◽  
Yasuji Ihara ◽  
...  

2000 ◽  
Vol 65 (11) ◽  
pp. 1726-1736 ◽  
Author(s):  
Miroslav Ledvina ◽  
Radka Pavelová ◽  
Anna Rohlenová ◽  
Jan Ježek ◽  
David Šaman

Carba analogs of normuramic acid, i.e., 3-(benzyl 2-acetamido-2,3-dideoxy-4,6-O-isopropylidene-α-D-glucopyranosid-3-yl)propanoic acid derivatives (nitrile or esters) 3a-3c were prepared by addition of radicals generated from benzyl 2-acetamido-2-deoxy-4,6-O-isopropylidene-3-O-[(methylsulfanyl)thiocarbonyl]- (2a) or -3-O-(phenoxythiocarbonyl)-α-D-glucopyranoside (2b) with Bu3SnH to acrylonitrile or acryl esters. Alkaline hydrolysis of ethyl ester 3c afforded 3-(benzyl 2-acetamido-2,3-dideoxy-4,6-O-isopropylidene-α-D-glucopyranosid-3-yl)propanoic acid (5). Coupling of acid 5 with L-2-aminobutanoyl-D-isoglutamine benzyl ester trifluoroacetate and subsequent deprotection of the intermediate 6 furnished N-[3-(2-acetamido-2,3-dideoxy-α-D-glucopyranosid-3-yl)propanoyl]-L-2-aminobutanoyl-D-isoglutamine (7).


2021 ◽  
pp. 112408
Author(s):  
Elizabeth Undiano ◽  
Susana Chávez ◽  
Pedro Mederos ◽  
Marcela Ayala ◽  
Antonio Monroy-Noyola

1987 ◽  
Vol 16 (2) ◽  
pp. 355-356 ◽  
Author(s):  
Sotaro Miyano ◽  
Kan Kawahara ◽  
Yoshio Inoue ◽  
Harukichi Hashimoto

Sign in / Sign up

Export Citation Format

Share Document