Novozym 435-catalyzed regioselective benzoylation of 1-β-D-arabinofuranosylcytosine in a co-solvent mixture of C4MIm·PF6 and pyridine

Biocatalysis and Biotransformation

Volumn 25, Issue 5, 2007, Pages 408-413

  Tan, Zi Yang ^a   Wu, Hong ^a   Zong, Min Hua ^a  

^a SOUTH CHINA UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

1 d arabinofuranosylcytosine; Enzymatic acylation; Ionic liquids; Regioselectivity; Vinyl benzoate

Indexed keywords

CO-SOLVENT MIXTURE; ENZYMATIC ACYLATION; REGIOSELECTIVE BENZOYLATION; VINYL BENZOATE;

ACYLATION; ENZYMES; IONIC LIQUIDS; PYRIDINE; REGIOSELECTIVITY; SOLVENTS;

BIOCATALYSTS;

1 BUTYL 3 METHYLIMIDAZOLIUM HEXAFLUOROPHOSPHATE; 5' O BENZOYLCYTARABINE; BENZOIC ACID DERIVATIVE; CYTARABINE; CYTARABINE DERIVATIVE; IONIC LIQUID; LIPASE B; ORGANIC SOLVENT; PYRIDINE; UNCLASSIFIED DRUG; VINYLBENZOIC ACID;

ACYLATION; ARTICLE; BIOTRANSFORMATION; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CHEMICAL REACTION KINETICS; CONTROLLED STUDY; DRUG STRUCTURE; DRUG SYNTHESIS; STRUCTURE ANALYSIS;

ARA;

EID: 35148895112     PISSN: 10242422     EISSN: 10292446     Source Type: Journal    
DOI: 10.1080/10242420701510635     Document Type: Article

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