1951
DOI: 10.1021/cr60151a002
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The Chemistry of the Benzimidazoles.

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1953
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Cited by 435 publications
(182 citation statements)
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“…For the applications of benzimidazole derivatives, see : Horton et al (2003); Wang et al (1994); Cowan (1998); Liu et al (2004Liu et al ( , 2011Wright (1951). For a related crystal structure, see: Huang et al (2010).…”
Section: Related Literaturementioning
confidence: 99%
“…For the applications of benzimidazole derivatives, see : Horton et al (2003); Wang et al (1994); Cowan (1998); Liu et al (2004Liu et al ( , 2011Wright (1951). For a related crystal structure, see: Huang et al (2010).…”
Section: Related Literaturementioning
confidence: 99%
“…There are several classical methods in the literature to obtain 1,3-benzazoles which involves the condensation reactions of either o-phenylenediamine, o-aminobenzenethiol, or o-aminophenol with substituted carboxylic acids, aldehydes, acyl chlorides, or nitriles [9][10][11][12][13][14][15]. Alternatively, benzimidazoles have also been synthesized using transition-metal catalyzed amination followed by condensation [16] and cyclization of o-nitroaniline derivatives with aryl isothiocyanates [17].…”
Section: Introductionmentioning
confidence: 99%
“…A variety of benzimidazoles are in used, like Thiabendazole, Flubendazole (antihelminthic), Omeprazole, Lansoprazole (anti-ulcerative) and Astemizole (anti-histaminic). The chemistry and pharmacology of benzimidazoles have been of great interest to medicinal chemistry [7,8] , because of its derivatives possessed various biological activities such as anti-oxidant [9,10], anti-microbial [11][12][13][14][15][16] , antihelmentic [17][18][19], anti-cancer [20], anti-hypertensive [21], anti-neoplastic [22], anti-inflammatory [23,24], analgesic [25], anti-protozoal [26,27], anti hepatitis activities [28] and also shows anti-depressant activity [29].…”
Section: Introductionmentioning
confidence: 99%