99388-23-5Relevant academic research and scientific papers
Regioselective synthesis of novel mono-substituted d-lactose fatty acid ester derivatives
Narouza, Mina R.,Soliman, Sameh E.,Bassily, Rafik W.,El-Sokkary, Ramadan I.,Nasr, Adel Z.,Nashed, Mina A.
, p. 502 - 509 (2013/08/23)
Three regioisomers of lactose fatty acid monoesters at positions 3', 6' and 3 and other related compounds have been chemically synthesized. The 3'- and 6'-O-palmitoyl-D-lactose derivatives were prepared via the regioselective esterification at O-3' and O-
4-O-beta-D-Galactopyranosyl-3-O-methyl-D-glucose: a new synthesis and application to the evaluation of intestinal lactase.
Fernandez-Mayoralas,Martin-Lomas,Villanueva
, p. 81 - 91 (2007/10/02)
4-O-beta-D-Galactopyranosyl-3-O-methyl-D-glucose (1, 3-O-methyl-lactose) has been prepared from benzyl 2,6-di-O-benzyl-4-O-(2,6-di-O-benzyl-3, 4-O-isopropylidene-beta-D-galactopyranosyl)-beta-D-glucopyranoside (5) and from benzyl 2,6-di-O-benzyl-4-O-(2,3,
