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Volumn 67, Issue 1-2, 2010, Pages 78-84
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Lipase-catalyzed enantio- and regioselective transformation of 3-epi-shikimic acid derivatives as the key step for the entry of polyoxygenated carbacycles
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KEIO UNIVERSITY
(Japan)
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Author keywords
Kinetic resolution; Lipase; Regioselective transformation; Transesterification
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Indexed keywords
CANDIDA ANTARCTICA LIPASE B;
DIHYDROXYLATION;
ENANTIO;
ENANTIOSELECTIVE;
HYDROXY GROUPS;
KINETIC RESOLUTION;
LIPASE-CATALYZED;
NATURALLY OCCURRING;
NOVOZYM435;
REGIO-SELECTIVE;
REGIOSELECTIVE TRANSFORMATION;
SELECTIVE TRANSFORMATION;
SHIKIMATES;
SHIKIMIC ACIDS;
STEREO-SELECTIVE;
SUBSTITUTION PATTERNS;
CARBOXYLIC ACIDS;
CATALYSIS;
ENANTIOSELECTIVITY;
ISOMERS;
TRANSESTERIFICATION;
REGIOSELECTIVITY;
3 EPI SHIKIMIC ACID DERIVATIVE;
CANDIDA ANTARCTICA LIPASE B;
CARBOXYLIC ACID DERIVATIVE;
METHYL (1,2,3,4,5) 3,4 DIACETOXY 5 (TERT BUTYLDIMETHYL) SILYLOXY 1,2 DIHYDROXYCYCLOHEXANECARBOXYLATE;
METHYL 3,4 DI O ACETYL 5 O (TERT BUTYLDIMETHYL)SILYL 3 EPI SHIKIMATE;
METHYL 3,4,5 TRI O ACETYLSHIKIMATE;
METHYL(3,4,5) 3,4,5 TRIACETOXY 1 CYCLOHEXENECARBOXYLATE;
SHIKIMIC ACID DERIVATIVE;
TRIACYLGLYCEROL LIPASE;
UNCLASSIFIED DRUG;
ARTICLE;
CATALYSIS;
DRUG ACETYLATION;
DRUG HYDROXYLATION;
DRUG TRANSFORMATION;
ENANTIOMER;
ENANTIOSELECTIVITY;
ENZYME MECHANISM;
NONHUMAN;
SUBSTITUTION REACTION;
TRANSESTERIFICATION;
CANDIDA ANTARCTICA;
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EID: 77956910133
PISSN: 13811177
EISSN: None
Source Type: Journal
DOI: 10.1016/j.molcatb.2010.07.009 Document Type: Article |
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Times cited : (5)
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References (13)
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