463934-93-2Relevant academic research and scientific papers
Facile synthesis of 1-thio-β-lactoside clusters scaffolded onto p-methoxyphenyl, β-D-galactopyranoside, β-D-glucopyranoside, and lactoside
Meng, Xiang-Bao,Yang, Lian-Dai,Li, Hui,Li, Qing,Cheng, Tie-Ming,Cai, Meng-Shen,Li, Zhong-Jun
, p. 977 - 981 (2002)
The free-radical addition of 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1 →4)-2,3,6-tri-O-acetyl-1-thio-β-D-glucopyranose to the allyl ether functions of p-methoxyphenyl per-O-allyl-D-galactopyranoside, D-glucopyranoside, and lactoside provides a concise and effective route for synthesis of glycoside clusters, of use for exploring anti-metastatic activity.
