An improved regioselective preparation of methyl 2,3-di-O-acetyl-α, β-d-xylofuranoside
Methyl 2,3-di-O-acetyl-α,β-d-xylofuranoside was prepared as the sole regioisomer in 6372% yield, according to the applied mass of substrate, through a Candida antarctica lipase B catalysed alcoholysis of methyl 2,3,5-tri-O-acetyl-α,β-d-xylofuranoside. The product is a potential synthetic precursor f...
Published in: | Biocatalysis and Biotransformation |
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Main Authors: | , , |
Format: | Article in Journal/Newspaper |
Language: | English |
Published: |
Taylor & Francis Ltd
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Subjects: | |
Online Access: | http://hdl.handle.net/11336/194493 |