V. A. Ogurtsov, O. A. Rakitin, Ch. W. Rees, A. A. Smolentsev, “4,5-Dichloro-1,2-dithiole-3-thione in the synthesis of benzimidazole, benzoxazole and benzothiazole derivatives of 1,3-dithioles”, Mendeleev Commun., 13:2 (2003), 50

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Mendeleev Communications, 2003, Volume 13, Issue 2, Pages 50–51
DOI: https://doi.org/10.1070/MC2003v013n02ABEH001750 (Mi mendc3951)

This article is cited in 19 scientific papers (total in 19 papers)

4,5-Dichloro-1,2-dithiole-3-thione in the synthesis of benzimidazole, benzoxazole and benzothiazole derivatives of 1,3-dithioles

V. A. Ogurtsov^a, O. A. Rakitin^a, Ch. W. Rees^b, A. A. Smolentsev^a

^a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
^b Department of Chemistry, Imperial College London, London, UK

Full-text PDF (100 kB) Citations (19)

DOI: https://doi.org/10.1070/MC2003v013n02ABEH001750

Abstract: 4,5-Dichloro-1,2-dithiole-3-thione 2 undergoes a 1,3-dipolar cycloaddition with DMAD to give stable aliphatic thioacyl chloride 3, which is highly reactive towards nucleophiles such as o-substituted amines to give benzimidazole, benzoxazole and benzothiazole derivatives of 1,3-dithioles 9.

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Document Type: Article

Language: English

Citation: V. A. Ogurtsov, O. A. Rakitin, Ch. W. Rees, A. A. Smolentsev, “4,5-Dichloro-1,2-dithiole-3-thione in the synthesis of benzimidazole, benzoxazole and benzothiazole derivatives of 1,3-dithioles”, Mendeleev Commun., 13:2 (2003), 50–51

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https://www.mathnet.ru/eng/mendc/v13/i2/p50

This publication is cited in the following 19 articles:

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