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 MoreAnhui New Star Pharmaceutical Development Co., Ltd
Contact:013956922763
Address:Floor 3, F9A, F Workshop, No.110 Kexue Road, High-Tech Development Zone, Hefei, Anhui ,China
Dalian RSD International Trade Co.,Ltd.(expird)
Contact:86-22-60875058 58610575
Address:Wantong International Areas, Hongqiao District, Tianjin, China.China
Suzhou Wedo Chemicals Co., Ltd.
Contact:86 512 58100425
Address:Zonger Road, DongSha Industry Park , Zhangjiagang, Jiangsu, China
Jiangxi Hito Chemical Co., Ltd.
Contact:+86-792-3170318
Address:No. 6, Tianhong Ave., Xinghuo Industry Park, Yongxiu, Jiujiang, Jiangxi, China
Nanjing Spring & Autumn Biological Engineering Co., Ltd.
Contact:86-180510-83338
Address:Suite# 210, No. 1 BuildingNanjing Agricultural Biotechnology High-tech Entrepreneurship Center, No. 4 Tongwei Road, Xuanwu District, Nanjing,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)