Maity_2008_J.Org.Chem_73_5629

Reference

Title : Efficient and selective enzymatic acylation reaction: separation of furanosyl and pyranosyl nucleosides - Maity_2008_J.Org.Chem_73_5629
Author(s) : Maity J , Shakya G , Singh SK , Ravikumar VT , Parmar VS , Prasad AK
Ref : J Org Chem , 73 :5629 , 2008
Abstract :

Candida antarctica lipase-B (CAL-B) immobilized on lewatite selectively acylated the primary hydroxyl group of the furanosyl nucleoside in a mixture of 1-(alpha-D-arabinofuranosyl)thymine and 1-(alpha-D-arabinopyranosyl)thymine. This selective biocatalytic acylation of furanosyl nucleoside has enabled us an easy separation of arabinofuranosyl thymine from an inseparable mixture with arabinopyranosyl thymine. The primary hydroxyl selective acylation methodology of arabinonucleoside has also been successfully used for the separation of 1-(beta-D-xylofuranosyl)thymine and 1-(beta-D-xylopyranosyl)thymine from a mixture of the two, which demonstrate the generality of the enzymatic methodology for separation of furanosyl and pyranosyl nucleosides.

PubMedSearch : Maity_2008_J.Org.Chem_73_5629
PubMedID: 18557651

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Citations formats

Maity J, Shakya G, Singh SK, Ravikumar VT, Parmar VS, Prasad AK (2008)
Efficient and selective enzymatic acylation reaction: separation of furanosyl and pyranosyl nucleosides
J Org Chem 73 :5629

Maity J, Shakya G, Singh SK, Ravikumar VT, Parmar VS, Prasad AK (2008)
J Org Chem 73 :5629