Email this article Regioselective Reduction of the C3=C3a Double Bond in 3-Aroylpyrrolo[1,2-c][4,1]benzoxazepine-1,2,4-triones
- Authors: Maslivets A.A.1, Maslivets A.N.1
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Affiliations:
- Perm State University
- Issue: Vol 55, No 10 (2019)
- Pages: 1621-1622
- Section: Short Communications
- URL: https://journal-vniispk.ru/1070-4280/article/view/221321
- DOI: https://doi.org/10.1134/S1070428019100269
- ID: 221321
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Abstract
The reaction of 3-aroyl-1H,6H-pyrrolo[1,2-c][4,1]benzoxazepine-1,2,4-triones with thioglycolic acid resulted in regioselective reduction of the C3=C3a bond with the formation of 3-aroyl-2-hydroxy-1H,6H-pyrrolo[1,2-c][4,1]benzoxazepine-1,4(3aH)-diones.
About the authors
A. A. Maslivets
Perm State University
Email: koh2@psu.ru
Russian Federation, Perm
A. N. Maslivets
Perm State University
Author for correspondence.
Email: koh2@psu.ru
Russian Federation, Perm
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