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Organic and Biomolecular Chemistry

Volumn 8, Issue 3, 2010, Pages 539-545

The thio-adduct facilitated, enzymatic kinetic resolution of 4-hydroxycyclopentenone and 4-hydroxycyclohexenone

(6) O'Byrne, Aisling a Murray, Cian a Keegan, Dearbhla a Palacio, Carole a Evans, Paul a Morgan, Ben S b

a UNIVERSITY COLLEGE DUBLIN (Ireland)

b UNIVERSITY OF LIVERPOOL (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DIASTEREOCONTROL; DIASTEREOSELECTIVE; ENANTIOMER RESOLUTION; ENANTIOMERIC EXCESS; ENZYMATIC KINETIC; ONE POT; SILYL ETHERS; STARTING MATERIALS; STEP SEQUENCES; VINYL ACETATES;

ENANTIOMERS; ETHERS;

CHIRALITY;

4 HYDROXYCYCLOHEXENONE; 4 HYDROXYCYCLOPENTENONE; 4-HYDROXYCYCLOHEXENONE; 4-HYDROXYCYCLOPENTENONE; CYCLOHEXANONE DERIVATIVE; CYCLOPENTANE DERIVATIVE; KETONE; SULFUR; TRIACYLGLYCEROL LIPASE;

ARTICLE; CANDIDA; CHEMISTRY; ENZYMOLOGY; KINETICS; METABOLISM; OXIDATION REDUCTION REACTION; STEREOISOMERISM; X RAY CRYSTALLOGRAPHY;

CANDIDA; CRYSTALLOGRAPHY, X-RAY; CYCLOHEXANONES; CYCLOPENTANES; KETONES; KINETICS; LIPASE; OXIDATION-REDUCTION; STEREOISOMERISM; SULFUR;

EID: 75149123868 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/b916506a Document Type: Article

Times cited : (22)

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