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Synthesis of 3-Aroylpyrrolo[1,2-a][4,1]benzoxazepine-1,2,4(6H)-triones by the Reaction of 2-(2-Aryl-2-oxoethylidene)­1,5-dihydro-4,1-benzoxazepin-3(2H)-ones with Oxalyl Chloride

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Abstract

The condensation of aroylpyruvic acids with o-aminobenzyl alcohol gave (Z)-2-(2-aryl-2-oxo­ethylidene)-1,5-dihydro-4,1-benzoxazepin-3(2H)-ones which reacted with oxalyl chloride to afford 3-aroylpyr­rolo­[1,2-a][4,1]benzoxazepine-1,2,4(6H)-triones.

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Funding

This study was performed under financial support by the Russian Science Foundation (project no. 19-13-00290).

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Authors and Affiliations

  1. Perm State University, 614990, Perm, Russia

    A. A. Maslivets, M. V. Dmitriev & A. N. Maslivets

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  1. A. A. Maslivets
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  2. M. V. Dmitriev
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  3. A. N. Maslivets
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Correspondence to A. N. Maslivets.

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Translated from Zhurnal Organicheskoi Khimii, 2021, Vol. 57, No. 10, pp. 1413–1419 https://doi.org/10.31857/S0514749221100062.

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Maslivets, A.A., Dmitriev, M.V. & Maslivets, A.N. Synthesis of 3-Aroylpyrrolo[1,2-a][4,1]benzoxazepine-1,2,4(6H)-triones by the Reaction of 2-(2-Aryl-2-oxoethylidene)­1,5-dihydro-4,1-benzoxazepin-3(2H)-ones with Oxalyl Chloride. Russ J Org Chem 57, 1608–1613 (2021). https://doi.org/10.1134/S1070428021100067

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