2011
DOI: 10.1016/j.tetlet.2011.03.046
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Ionic liquid supported multistep divergent synthesis of benzimidazole linked pyrrolo-/pyrido-/isoindolo-benzimidazolones

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Cited by 12 publications
(9 citation statements)
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“…3,4,4a,5-Tetrahydrobenzo [4,5]imidazo [1,2-a]pyridin-1(2H)-ones linked by benzimidazoles have also been documented. 16 The aromatic part of 1,2-dihydrobenzo [4,5]imidazo [1,2-a]pyrazin-3(4H)-ones II, benzimidazoles, were synthesized several times, in solution 17−21 and on solid phase. 22−25 Benzimidazole derivatives can serve as angiotensin II receptor antagonists, 26 as inhibitors of trypsinlike serine protease (factor Xa), 27 and as antibacterial agents.…”
Section: ■ Introductionmentioning
confidence: 99%
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“…3,4,4a,5-Tetrahydrobenzo [4,5]imidazo [1,2-a]pyridin-1(2H)-ones linked by benzimidazoles have also been documented. 16 The aromatic part of 1,2-dihydrobenzo [4,5]imidazo [1,2-a]pyrazin-3(4H)-ones II, benzimidazoles, were synthesized several times, in solution 17−21 and on solid phase. 22−25 Benzimidazole derivatives can serve as angiotensin II receptor antagonists, 26 as inhibitors of trypsinlike serine protease (factor Xa), 27 and as antibacterial agents.…”
Section: ■ Introductionmentioning
confidence: 99%
“…Other related derivatives, such as deazaanalogues of compound II , 1,2-dihydrobenzo[4,5]imidazo[1,2- a ]pyridin-3(5 H )-ones III (Figure ), are reportedly anxiolytic, antiviral, and antimicrobial agents. 3,4,4a,5-Tetrahydro­benzo[4,5]imidazo[1,2- a ]pyridin-1(2 H )-ones linked by benzimidazoles have also been documented . The aromatic part of 1,2-dihydrobenzo[4,5]imidazo[1,2- a ]pyrazin-3(4 H )-ones II , benzimidazoles, were synthesized several times, in solution and on solid phase. Benzimidazole derivatives can serve as angiotensin II receptor antagonists, as inhibitors of trypsin-like serine protease (factor Xa), and as antibacterial agents .…”
Section: Introductionmentioning
confidence: 99%
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“…IL-grafted 101 was selected as a common scaffold to the synthesis of 2-alkyl-substituted bis-benzimidazole 102, and pyrrole[1,2-a]benzimidazolones 103 using various keto acids in one step (Scheme 12) [43]. SCHEME 12 Sun's diversity-oriented approaches toward heterocycles-resembling compound libraries.…”
Section: Use Of Ionic Liquid-supported Diaminementioning
confidence: 99%
“…Benzimidazole heterocycles are well established as ''privileged scaffolds,'' being integrated into pharmaceutical agents to form enzyme inhibitors, receptor-binding drugs, and DNA intercalators [13,14]. Benzimidazole derivatives have been reported to possess noteworthy pharmacological activities such as anticancer [15], antimicrobial [16], antihypertensive [17], cytotoxic [18], anticonvulsant [19], antileukemic [20], and antifungal properties [21]. Recently, benzimidazole nucleuscontaining drugs cambendazole, thiabendazole, and mebendazole were reported to display antihelminthics activity [22] (Fig.…”
Section: Introductionmentioning
confidence: 99%