Monatshefte fur Chemie p. 709 - 712 (1990)
Update date:2022-08-29
Topics:
Reisch, Johannes
Wickramasinghe, Anura
Epoxidation of acridone alkaloid acronycine (1) resulted in hydroxylation at the aromatic ring giving 5-hydroxyacronycine (3).The same reaction on 1,3-dimethoxy-10-methyl-9(10H)-acridone (5) gave 1,3-dimethoxy-2-hydroxy-10-methyl-9(10H)-acridone (6), 1,3-dimethoxy-2-hydroxy-4-peroxy-10-methyl-9(10H)-acridone (8), and 1,3-dimethoxy-2,4-diperoxy-10-methyl-9(10H)-acridone (9).
View More
HUNAN CHEMAPI BIOLOGICAL TECHNOLOGY CO.,LTD.
Contact:+86-186-02659358
Address:1004, building 3, Wanke Jinsemaitianyuan, 498 Guitang Road, Yuhua District, Changsha City, Hunan Province, China
Shanghai Micro-mega Industry Co., Ltd.
Contact:0086-21-34628682;57153848
Address:Rm413,No.413,West Meilong Road, Minhang District,Shanghai P R China
Shanghai Send Pharmaceutical Technology Co., Ltd.
website:http://www.shsendpharma.com
Contact:021-58088081, +8613585868794
Address::Room A601, Building 1,NO. 800 Qingdai Road Pudong District Shanghai,China
website:http://www.arromax.com
Contact:+86-0512-62959601 skype:aimmezhang
Address:Suite 401, Bldg A3, 218 Xinghu St.Suzhou Industrial Park 215123, P.R. China
Contact:+86-579-85206992
Address:No 451 chouzhou north road ,room 1106 int'l business center , yiwu ,china
Doi:10.1021/jp054688j
(2006)Doi:10.1002/ejic.200390065
(2003)Doi:10.1063/1.104850
(1991)Doi:10.1021/acs.orglett.8b00439
(2018)Doi:10.1016/0022-328X(89)87228-6
(1989)Doi:10.1016/j.bmcl.2018.03.026
(2018)
