SPECIFIC SYNTHESIS AND STEREOCHEMICAL ASSIGNMENT OF THE DIASTEREOMERIC 3,5-O-BENZYLIDENE-1,2-O-ISOPROPYLIDENE-α-D-GLUCOFURANOSE ISOMERS

DOI: 10.1016/0008-6215(86)84012-5

Source and publish data:

Carbohydrate Research p. 137 - 146 (1986)

Update date:2022-07-29

Topics:

Authors:

Akerfeldt, Karin

Bartlett, Paul A.

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Article abstract of DOI:10.1016/0008-6215(86)84012-5

Pyridinium tosylate-catalysed acetal exchange between benzaldehyde dimethyl acetal and 6-O-(tert-butyldiphenylsilyl)-1,2-O-isopropylidene-α-D-glucofuranose was investigated as an alternative to the original procedure of Brigl and Gruener (condensation of

Full text of DOI:10.1016/0008-6215(86)84012-5

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