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Diels-Alder reactions of 3-and 5-methyl-1-vinylpyrazoles with cyclohexa-1,3-diene and hydrogenation of the reaction products

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Abstract

The behavior of isomeric vinylpyrazoles in the Diels-Alder reactions with cyclohexa-1,3-diene was studied to show that the spatial location of the vinyl group on the N2 atom does not affect the diene synthesis.

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Authors and Affiliations

  1. ARIAK Institute of Applied Chemistry, Artashatsoe shosse 5/2, Erevan, 375053, Armenia

    O. S. Attaryan

  2. Institute of Organic Chemistry, National Academy of Sciences of Armenia, Erevan, Armenia

    A. O. Baltayan & G. V. Asratyan

Authors
  1. O. S. Attaryan
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  2. A. O. Baltayan
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  3. G. V. Asratyan
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Correspondence to A. O. Baltayan.

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Original Russian Text © O.S. Attaryan, A.O. Baltayan, G.V. Asratyan, 2008, published in Zhurnal Obshchei Khimii, 2008, Vol. 78, No. 4, pp. 645–647.

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Attaryan, O.S., Baltayan, A.O. & Asratyan, G.V. Diels-Alder reactions of 3-and 5-methyl-1-vinylpyrazoles with cyclohexa-1,3-diene and hydrogenation of the reaction products. Russ J Gen Chem 78, 626–628 (2008). https://doi.org/10.1134/S1070363208040191

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  • DOI: https://doi.org/10.1134/S1070363208040191

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