892402-77-6Relevant articles and documents
Synthesis of mono- and di-O-β-D-glucopyranoside conjugates of (E)-resveratrol
Zhang, Zhaojun,Yu, Biao,Schmidt, Richard R.
, p. 1301 - 1306 (2007/10/03)
Starting from the commercially available natural product (E)-resveratrol (1), the four selectively tert-butyldimethylsilyl (TBS) protected (E)-resveratrols 6-9 were prepared by one reaction. Using 6-9 as glucosyl acceptors and trifluoroacetimidate 11 as glucosyl donor, three bioactive natural glucopyranoside conjugates of (E)-resveratrol 2-4 and one novel compound (5) were efficiently prepared in two steps. Georg Thieme Verlag Stuttgart.