Chemistry of Natural Compounds p. 181 - 186 (1993)
Update date:2022-08-03
Topics:
Pivovarenko, V. G.
Khilya, V. P.
The products of the interaction of α-acetobromoglucose with 2,4,5-trihydroxyphenyl benzyl ketone and 2,4-dihydroxyphenyl 4'-hydroxybenzyl ketone and also with their heterocyclic analogues, which are present completely or partially in the enolic form, have been investigated.It has been shown that in this reaction a tetra-O-acetylglucosyl residue is added at the 4-OH hydroxy group of the phenyl residue of the ketone.The compounds obtained have been converted into isoflavone 7-O-glucosides by the action of the Vilsmeier reagent or acetoformic anhydride.
View MoreTianjin Jiuri New Materials Co., Ltd.
Contact:+86-22-58889220
Address:C-5/6, Vison Hill, No.1 Gonghua Road, Huayuan Hi-tech Park, Tianjin, China.
Shandong Topscience Biotech Co., Ltd.
Contact:0633-2619278
Address:No. 98 Lanshan West Road, Lanshan District, Rizhao, Shandong Province, P.R. of China
Shandong Bolode Bio-Technology Co., LTD
Contact:+86-0531-58966870
Address:136 Jingyi Road,Huaiyin District,Jinan,Shandong,China
Contact:
Address:
SHENYANG COMEBOARD TECHNOLOGY CO., LTD
Contact:+86-24-25724626
Address:Room2210,Tianbao International Building,No.8-1 Weigong South Street,Tiexi District,Shenyang,China
Doi:10.1002/hlca.19950780711
(1995)Doi:10.1021/jo952189g
(1996)Doi:10.1021/ol034172n
(2003)Doi:10.1021/ja963827v
(1997)Doi:10.1016/0008-6215(95)00223-G
(1995)Doi:10.1002/ejoc.200300069
(2003)
