An improved procedure for the regioselective acetylation of monosaccharide derivatives by pancreatin-catalyzed transesterification in organic solvents

DOI: 10.1055/s-1991-26510

Source and publish data:

Synthesis p. 533 - 535 (1991)

Update date:2022-07-29

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Authors:

Theil Theil

Schick Schick

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Article abstract of DOI:10.1055/s-1991-26510

A series of pyranoside and furanosidic monosaccharide derivatives were monoacetylated in the 6-position with high regioselectivity and good to excellent yields by the pancreatin-catalyzed transesterification with vinyl acetate in the solvent system tetrahydrofuran/triethylamine.

Full text of DOI:10.1055/s-1991-26510

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Product name:Acetic acid (2R,3S,4S,5R,6R)-6-ethoxy-3,4,5-trihydroxy-tetrahydro-pyran-2-ylmethyl ester

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