A versatile one-step method for the synthesis of benzimidazoles from quinoxalinones and arylenediamines via a novel rearrangement

Tetrahedron Letters

Volumn 49, Issue 31, 2008, Pages 4644-4647

  Mamedov, Vakhid A ^a   Saifina, Dina F ^a   Rizvanov, Il'dar Kh ^a   Gubaidullin, Aidar T ^a  

^a A E ARBUZOV INSTITUTE OF ORGANIC AND PHYSICAL CHEMISTRY   (Russian Federation)

Author keywords

1,2 Arylenediamines; Benzimidazole; Quinoxaline; Rearrangement; Ring contraction

Indexed keywords

3 ALKANOYLQUINOXALIN 2 ONE; 3 AROYLQUINOXALIN 2 ONE; BENZIMIDAZOLE DERIVATIVE; DIAMINE DERIVATIVE; QUINOXALINE DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG STRUCTURE; DRUG SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE; X RAY CRYSTALLOGRAPHY;

EID: 45049087698     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.05.060     Document Type: Article

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35. -3). Crystallographic data (excluding structure factors) for structure 3h in this Letter have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 683079. Copies of these data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK, (fax: +44-(0)1223-336033 or e-mail: deposit@ccdc.cam.ac.uk). Deposited data may be accessed by the journal and checked as part of the refereeing process.