The use of vinyl esters significantly enhanced enantioselectivities and reaction rates in lipase-catalyzed resolutions of arylaliphatic carboxylic acids

被引:60
作者
Yang, H [1 ]
Henke, E [1 ]
Bornscheuer, UT [1 ]
机构
[1] Univ Stuttgart, Inst Tech Biochem, D-70569 Stuttgart, Germany
关键词
D O I
10.1021/jo981780l
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
引用
收藏
页码:1709 / 1712
页数:4
相关论文
共 23 条
[1]  
AMAKI Y, 1994, APPL MICROBIOL BIOT, V40, P664, DOI 10.1007/s002530050047
[2]   Calculation of enantiomer ratio and equilibrium constants in biocatalytic ping-pong bi-bi resolutions [J].
Anthonsen, HW ;
Hoff, BH ;
Anthonsen, T .
TETRAHEDRON-ASYMMETRY, 1996, 7 (09) :2633-2638
[3]   FACTORS AFFECTING THE LIPASE-CATALYZED TRANSESTERIFICATION REACTIONS OF 3-HYDROXY ESTERS IN ORGANIC-SOLVENTS [J].
BORNSCHEUER, U ;
HERAR, A ;
KREYE, L ;
WENDEL, V ;
CAPEWELL, A ;
MEYER, HH ;
SCHEPER, T ;
KOLISIS, FN .
TETRAHEDRON-ASYMMETRY, 1993, 4 (05) :1007-1016
[4]   ASYMMETRIC-SYNTHESIS AND STRUCTURAL-ANALYSIS OF 5-O-BENZOYL-2,3-DIDEOXY-3-FLUORO-ALPHA,BETA-D-RIBOFURANOSE AND 5-O-BENZOYL-2,3-DIDEOXY-3-FLUORO-ALPHA,BETA-D-XYLOFURANOSE FROM HOMOCHIRAL 1-FLUORO-3-SULFINYLACETONE [J].
BRAVO, P ;
PIOVOSI, E ;
RESNATI, G ;
FRONZA, G .
JOURNAL OF ORGANIC CHEMISTRY, 1989, 54 (21) :5171-5176
[5]   QUANTITATIVE-ANALYSES OF BIOCHEMICAL KINETIC RESOLUTIONS OF ENANTIOMERS [J].
CHEN, CS ;
FUJIMOTO, Y ;
GIRDAUKAS, G ;
SIH, CJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (25) :7294-7299
[6]   ENZYMATIC-REACTIONS IN ORGANIC-SYNTHESIS .2. ESTER INTERCHANGE OF VINYL ESTERS [J].
DEGUEILCASTAING, M ;
DEJESO, B ;
DROUILLARD, S ;
MAILLARD, B .
TETRAHEDRON LETTERS, 1987, 28 (09) :953-954
[7]  
GABER K, 1997, BIOTRANSFORMATIONS O
[8]  
HELMCHEN G, 1977, TETRAHEDRON LETT, P1417
[9]   DRASTIC SOLVENT EFFECT ON LIPASE-CATALYZED ENANTIOSELECTIVE HYDROLYSIS OF PROCHIRAL 1,4-DIHYDROPYRIDINES [J].
HIROSE, Y ;
KARIYA, K ;
SASAKI, I ;
KURONO, Y ;
EBIIKE, H ;
ACHIWA, K .
TETRAHEDRON LETTERS, 1992, 33 (47) :7157-7160
[10]  
Kazlauskas R.J., 1998, BIOTECHNOLOGY, P37, DOI [DOI 10.1002/9783527620999.CH3H, 10.1002/9783527620999.ch3h]