
Chemistry of Heterocyclic Compounds p. 325 - 330 (1994)
Update date:2022-07-29
Topics: Synthesis Yield Electrophile Nucleophilic substitution Leaving group Reaction Conditions Heterocyclic compound Solvent system Spectroscopic analysis (NMR, IR, MS) Reactivity study Chromatography (TLC, HPLC)
Anisimova, V. A.
Lukova, O. A.
Treatment of 2-aminobenzimidazoles with 1,3-dichloroacetone or radical bromination of 3-alkoxycarbonyl- or 3-acetyl-2-methylimidazo<1,2-a>benzimidazoles leads to the 2-halomethyl derivatives of this heterocycle.The lability of the halogen atom in the synt
View MoreShandong Jincheng Zhonghua Bio-pharmaceutical Co.,Ltd
Contact:+86-533-5415882
Address:Zichuan Economic Development Zone,Zibo City,Shandong Province,China
SHANGHAI RC CHEMICALS CO.,LTD.
website:http://www.rcc.net.cn
Contact:+86-21-50322175
Address:Rm1415 Yinqiao Masion No.58 Jinxin Road Pudong Shanghai China
Shanghai Run-Biotech Co., Ltd.
website:http://www.run-biotech.com
Contact:+86-21-31576854/57171705 / 57171706
Address:second floor, building 3, No.999, jiangyue Road, minghang District, Shanghai, China
Hebei Tianxiang Biological & Pharmaceutical Co., Ltd
Contact:86-0312-6615158
Address:No 42 fazhan street qingyuan county
Shanghai Kefu Chemical Co.,Ltd.
Contact:+86-21-34616196
Address:Room601-602, Xuhui Business Building, No.168, Yude Road, Shanghai
Doi:10.1080/00397911.2010.535947
(2012)Doi:10.1021/np034028a
(2004)Doi:10.1081/NCN-100105239
(2001)Doi:10.1002/zaac.19966220307
(1996)Doi:10.1039/c3tb20156b
(2013)Doi:10.1016/0008-6215(95)00014-K
(1995)