
Chemistry of Heterocyclic Compounds p. 459 - 461 (1996)
Update date:2022-08-22
Topics:
Varlamov
Krapivko
N'ende
Levov
Prostakov
The possibility of synthesis of quinoline[1,2-a]benzimidazole from aniline and quinoline on a dehydrogenating mark K-16 catalyst at 560-580°C was demonstrated. It was established that in the nitration of quinolino[1,2-a]benzimidazole, a 10-nitro-derivative is formed, whereas in the reaction with ADCE, tetramethoxycarbonylquinolino[1,2-a]pyrido[2′,1′-b]benzimidazole is formed. 1996 Plenum Publishing Corporation.
View More
ShenZhen InnoSyn Biotech Co.,Ltd
website:http://www.innosyns.com
Contact:+86-755-28351685
Address:Floor 5 & 6, Building A1, HAIKEXING Strategic Innovative Industrial Park, 16 BaoShan Road, PingShan District
Nanjing Fayekong Chemcial Co.,Ltd(expird)
Contact:86-25-58813444
Address:Rm 1503, Unit 1, Building 5, Zijinnanyuan, Nanjing, Jiangsu, China
SHIJIAZHUANG HENRYTE CHEMICALS CO,.LTD(expird)
Contact:+86-311-85208698 311-80837698
Address:NO.166, yuhua west road, SHIJIAZHUANG, China
shanghai tuomiao chemicial co.,ltd.
website:https://www.tuomiaochem.com/
Contact:021 - 59853336
Address:shanghai
Contact:+86 21 5017 5386
Address:No 999,Jiangyue Rd, Minhang Dist ,201114,Shanghai ,China
Doi:10.1021/jo01089a022
(1959)Doi:10.3390/molecules15053276
(2010)Doi:10.1016/j.catcom.2013.11.003
(2014)Doi:10.1039/jr9630002351
(1963)Doi:10.1016/0022-1139(94)03084-D
(1995)Doi:10.3987/COM-16-13484
(2016)