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Volumn 4, Issue 5-6, 1998, Pages 295-302
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Enzymatic alcoholysis of SO2-uracil analog diacyclonucleosides. Long- distance effect of the substituents on the regioselectivity
a
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Author keywords
Acyclonucleoside; Alcoholysis; Lipase; Regioselectivity; Thiadiazine
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Indexed keywords
CATALYSIS;
COMPOSITION EFFECTS;
ELECTRONIC STRUCTURE;
HYDROGEN BONDS;
MOLECULAR STRUCTURE;
SULFUR DIOXIDE;
ACYCLONUCLEOSIDE;
ENZYMATIC ALCOHOLYSIS;
LIPASE;
REGIOSELECTIVITY;
THIADIAZINE;
URACIL;
ENZYMES;
CARBONYL DERIVATIVE;
CYCLOPROPANE;
HYDROGEN;
HYDROXYL GROUP;
NUCLEOSIDE;
THIADIAZINE DERIVATIVE;
TRIACYLGLYCEROL LIPASE;
URACIL DERIVATIVE;
ARTICLE;
DEGRADATION;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
HYDROGEN BOND;
NUCLEAR MAGNETIC RESONANCE;
STEREOSPECIFICITY;
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EID: 0032479814
PISSN: 13811177
EISSN: None
Source Type: Journal
DOI: 10.1016/S1381-1177(98)00068-X Document Type: Article |
Times cited : (3)
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References (14)
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