Journal of Organic Chemistry p. 386 - 389 (1981)
Update date:2022-08-03
Topics:
Manikumar, Govindarajan
Shamma, Maurice
Dichlorocarbene adds to oxyberberine (2) to furnish the key adduct 5.Hydrolysis of 5 in dilute hydrochloric acid yields oxyberberine-13-carboxaldehyde (7).Reduction of adduct 5 with zinc in acetic acid produces 13-methyloxyberberine (11).Alternatively, reduction of 5 with lithium aluminum hydride in hot THF leads to enlargement of ring C with formation of the vinylic chloride 14.A complex transformation occurs when 5 is refluxed in aqueous pyridine, the product being keto lactam 15.Dichlorocarbene in chloroform also adds to berberine (1) to form pentachloro derivative 22.Acid hydrolysis of 22 gives rise to aldehyde 23 which loses hydrogen chloride in the presence of silver oxide to afford dichloro compound 25.Sodium borohydride reduction of 23 produces alcohol 24.
View MoreContact:13813902930 025-52714267
Address:20 Fengji Road, Yuhua Economic Development Zone, Nanjing, Jiangsu, P. R. China
Xi'an Tizan Tech & Industry Co., Ltd.
Contact:86-18629066522
Address:C3009 TANG FENG INTERNATIONAL PLAZA, NO.18 FENGHUI NAN ROAD, XI'AN HIGH TECH ZONE, 710075 CHINA.
Tianjin Realet Chemical Technology Co.,Ltd.
website:http://www.realetchem.com
Contact:+86-022-58788819
Address:shuanggang industrial park
Shanghai Witshoot Internet Technology Co Ltd
Contact:+86-21-66390020
Address:Room 419, No.285 Luochuan Road (E)
Zhonghao (dalian) Research and Design Institute of Chemical Industry Co., Ltd
Contact:+86 411 84674606
Address:201, Huangpu Road , Shahekou District, Dalian ,116023-China
Doi:10.1002/hc.10222
(2004)Doi:10.1016/S0040-4039(01)01780-4
(2001)Doi:10.1039/P29890001623
(1989)Doi:10.1016/S0040-4039(00)83894-0
(1986)Doi:10.1021/ja00512a051
(1979)Doi:10.1016/j.tetlet.2004.06.072
(2004)