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
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Doi:10.1080/00397911.2010.535947
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(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)
