Archiv der Pharmazie p. 790 - 794 (1980)
Update date:2022-08-04
Topics:
Pindur, Ulf
The 3-substituted indoles 1 and 2 react with 2,6-dimethoxybenzaldehyde (3a) to yield the diindolylmethanes 4 and 6 by acid catalysis.The reaction of 2 with 3a also yields the tetrahydro-β-carboline 7.The sterically hindered mesitylaldehyde (3b) reacts only with the indole 1 to give the 2,2'-diindolylmethane 5, while the tryptophane methyl ester 2 yields the tetrahydro-β-carboline 8 only.
View MoreWuhan Konberd Biotech Co., Ltd.
Contact:+86-27-87205925
Address:NO.666, Gaoxin Road, Eastlake High-tech zone
Changsha Goomoo Chemical Technology Co.Ltd
Contact:+86-731-82197655
Address:No.649,Chezhan Rd.(N),Changsha,Hunan,China
Contact:0833-5590788/5590338/5590055
Address:Victory in the town of Red Star Village,Mount Emei City,industrial concentration area storage processing logistics parkpark
Hubei Honch Pharmaceutical Co.,Ltd
Contact:86-713-7222018
Address:Li Shizhen Pharmaceutical Industry park, Qichun County, Hubei Province,China
Contact:021
Address:Pudong
Doi:10.1021/acs.jmedchem.6b01879
(2017)Doi:10.1016/j.bmcl.2011.05.091
(2011)Doi:10.1016/j.bmcl.2004.06.046
(2004)Doi:10.1016/S0022-328X(00)83863-2
(1980)Doi:10.1039/c9sc00711c
(2019)Doi:10.1021/jo202269p
(2012)
