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Dipyrrolo[1,2-a:2',1'-c]pyrazines. 8. Electrophilic Substitution in Dipyrrolo[1,2-a:2',1'-c]pyrazines and 5,6-Dihydrodipyrrolo[1,2-a:2',1'-c]pyrazines. Acylation of Dipyrrolo[1,2-a:2',1'-c]pyrazines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Esters, nitriles, and amides of dipyrrolo[1,2-a:2',1'-c]pyrazines have been synthesized by the acylation of dipyrrolo[1,2-a:2',1'-c]pyrazines and 5,6-dihydrodipyrrolo[1,2-a:2',1'-c]pyrazines with trichloroacetic acid chloride, p-tosyl isocyanate, and isocyanatophosphoric acid dichloride (Kirsanov isocyanate).

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Authors and Affiliations

  1. Moscow M. V. Lomonosov State University, Moscow, 119899, Russia

    V. I. Terenin, E. A. Sumtsova, E. V. Kabanova & N. V. Zyk

  2. A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences (RAN), Moscow, 119991

    A. P. Pleshkova

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  1. V. I. Terenin
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  2. E. A. Sumtsova
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  3. E. V. Kabanova
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  4. A. P. Pleshkova
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  5. N. V. Zyk
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Terenin, V.I., Sumtsova, E.A., Kabanova, E.V. et al. Dipyrrolo[1,2-a:2',1'-c]pyrazines. 8. Electrophilic Substitution in Dipyrrolo[1,2-a:2',1'-c]pyrazines and 5,6-Dihydrodipyrrolo[1,2-a:2',1'-c]pyrazines. Acylation of Dipyrrolo[1,2-a:2',1'-c]pyrazines. Chemistry of Heterocyclic Compounds 40, 436–445 (2004). https://doi.org/10.1023/B:COHC.0000033534.04746.70

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  • DOI: https://doi.org/10.1023/B:COHC.0000033534.04746.70

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