ChemInform Abstract: Membrane-Enclosed Enzymatic Catalysis (MEEC): A Useful, Practical New Method for the Manipulation of Enzymes in Organic Synthesis.

ChemInform ◽  
1987 ◽  
Vol 18 (27) ◽  
Author(s):  
M. D. BEDNARSKI ◽  
H. K. CHENAULT ◽  
E. S. SIMON ◽  
G. M. WHITESIDES
Keyword(s):  
Organic Synthesis ◽  
Enzymatic Catalysis ◽  
New Method ◽  
Enzymes In Organic Synthesis

Membrane-enclosed enzymic catalysis (MEEC): a useful, practical new method for the manipulation of enzymes in organic synthesis

1987 ◽  
Vol 109 (4) ◽  
pp. 1283-1285 ◽  
Author(s):  
Mark D. Bednarski ◽  
H. Keith Chenault ◽  
Ethan S. Simon ◽  
George M. Whitesides
Keyword(s):  
Organic Synthesis ◽  
New Method ◽  
Enzymes In Organic Synthesis

Enzymes in organic synthesis. 33. Stereoselective pig liver esterase-catalyzed hydrolyses of meso cyclopentyl-, tetrahydrofuranyl-, and tetrahydrothiophenyl-1,3-diesters

1985 ◽  
Vol 63 (2) ◽  
pp. 452-456 ◽  
Author(s):  
J. Bryan Jones ◽  
R. Scott Hinks ◽  
Philip G. Hultin
Keyword(s):  
Organic Synthesis ◽  
Absolute Configuration ◽  
Enantiomeric Excess ◽  
Membered Ring ◽  
Pig Liver ◽  
Pig Liver Esterase ◽  
Preparative Scale ◽  
Liver Esterase ◽  
The Absolute ◽  
Enzymes In Organic Synthesis

Preparative-scale pig liver esterase-catalyzed hydrolyses of five-membered ring meso-1,3-diesters are enantiotopically selective. While pro-S enantiotopic selectivity is exhibited in each case, the absolute configuration sense of the hydrolysis in the cyclopentyl series is opposite to that of both the tetrahydrofuranyl and tetrahydrothiophenyl diesters. The enantiomeric excess levels induced are in the 34–46% range.

Esterolytic and Lipolytic Enzymes in Organic Synthesis

Synthesis ◽  
1991 ◽  
Vol 1991 (12) ◽  
pp. 1049-1072 ◽  
Author(s):  
Wilhelm Boland ◽  
Christian Frößl ◽  
Michael Lorenz
Keyword(s):  
Organic Synthesis ◽  
Lipolytic Enzymes ◽  
Enzymes In Organic Synthesis

ChemInform Abstract: Enzymes in Organic Synthesis: Oxidoreductions.

ChemInform ◽  
2010 ◽  
Vol 26 (33) ◽  
pp. no-no
Author(s):  
J.-M. FANG ◽  
C.-H. LIN ◽  
C. W. BRADSHAW ◽  
C.-H. WONG
Keyword(s):  
Organic Synthesis ◽  
Enzymes In Organic Synthesis

Enzymes in organic synthesis. 32. Stereospecific horse liver alcohol dehydrogenase-catalyzed oxidations of exo- and endo-oxabicyclic meso diols

1984 ◽  
Vol 62 (11) ◽  
pp. 2578-2582 ◽  
Author(s):  
J. Bryan Jones ◽  
Christopher J. Francis
Keyword(s):  
Alcohol Dehydrogenase ◽  
Organic Synthesis ◽  
Horse Liver Alcohol Dehydrogenase ◽  
Preparative Scale ◽  
Enantiomerically Pure ◽  
Liver Alcohol Dehydrogenase ◽  
Horse Liver ◽  
One Step ◽  
Catalyzed Oxidation ◽  
Enzymes In Organic Synthesis

Preparative-scale horse liver alcohol dehydrogenase-catalyzed oxidation of mesoexo- and endo-7-oxabicyclo[2.2.1]heptane diols provides a direct one-step route to enantiomerically pure chiral γ-lactones of the oxabicyclic series.

New Method and Reagents in Organic Synthesis. 87. Reaction of Trimethylsilyldiazomethane with Quinones

Heterocycles ◽  
1990 ◽  
Vol 30 (1) ◽  
pp. 375 ◽  
Author(s):  
Takayuki Shioiri ◽  
Toyohiko Aoyama ◽  
Takao Nakano ◽  
Satoshi Nishigaki
Keyword(s):  
Organic Synthesis ◽  
New Method
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