Open AccessPreparation of some D-glucofuranosides from unprotected D-glucose
Author(s) -
D. Joniak,
Monika Poláková
Publication year - 2001
Publication title -
journal of the serbian chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.227
H-Index - 45
eISSN - 1820-7421
pISSN - 0352-5139
DOI - 10.2298/jsc0102081j
Subject(s) - anhydrous , chemistry , vanillin , alcohol , chloride , ferric , benzyl alcohol , organic chemistry , medicinal chemistry , catalysis
O-Glycosidation of 3-(4-methoxyphenyl) propyl alcohol, benzyl alcohol and vanillin with totally unprotected D-glucose, performed in a heterogeneous media and promoted by anhydrous ferric chloride, afforded competent D-glucofuranosides as the major and D-glucopyranosides as the minor products of the reaction.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom