Journal of Medicinal Chemistry p. 798 - 806 (1991)
Update date:2022-08-05
Topics: Synthesis IC50 Scaffold Analogues Inhibitor Docking Studies Structure-Activity Relationship (SAR) Phosphorylation In vitro assay Flavonoid Chromatography (HPLC, TLC) Cell proliferation assay Spectroscopy (NMR, IR, MS)
Cushman, Mark
Nagarathnam, Dhanapalan
Burg, Debra L.
Geahlen, Robert L.
Treatment of o-hydroxyacetophenones 2a-e with excess lithium bis(trimethylsilyl)amide followed by dialkyl carbonates gave 3-(2-hydroxyaryl)-3-oxopropanoates 3a-e.The latter substances were transformed through the reaction of their magnesium chelates with
View MoreChengdu CSH Pharmaceutical Co.,ltd
Contact:+86-(28)-85321971
Address:Block B,New Hope Int. Tian Fu New District, Chengdu, Sichuan, China
Zhejiang Kente Chemical Co.,Ltd.
Contact:86-0576-87651912
Address:No.7, Fengxi West Road, Modern Industrial Zone
TIANJIN FESTO CHEMICAL CO.,LTD(expird)
Contact:86-22-25814570
Address:No.12th,5th Ave.,TEDA,Tianjin,China
Hangzhou GreenCo Science & Technology Co., Ltd.
Contact:86-571-88257303
Address:1713 Room,Jingui Building,Gudun Road,Xihu District,Hangzhou,China
Beijing Century Richap Chemistry Co.,Ltd
Contact:+86- 010-64455497
Address:Guannan County, Lianyungang City, Jiangsu Province, China
Doi:10.1021/jo00892a008
(1975)Doi:10.1021/ol034218c
(2003)Doi:10.1021/acs.inorgchem.0c01669
(2020)Doi:10.1007/BF01418005
(1981)Doi:10.1248/yakushi1947.96.6_810
(1976)Doi:10.1002/anie.201300459
(2013)
