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Synthesis of isoxazolo[4,5-e][1,4]diazepin-5-ones from 5-acyl-4-(haloacetylamino)isoxazoles

Victor Petrovich Kislyi 1
Victor Petrovich Kislyi
Evgenia Borisovna Danilova 1
Evgenia Borisovna Danilova
Victor Vladimirovich Semenov 1
Victor Vladimirovich Semenov
Published 2012-02-27
CommunicationVolume 22, Issue 2, 85-86
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Kislyi V. P., Danilova E. B., Semenov V. V. Synthesis of isoxazolo[4,5-e][1,4]diazepin-5-ones from 5-acyl-4-(haloacetylamino)isoxazoles // Mendeleev Communications. 2012. Vol. 22. No. 2. pp. 85-86.
GOST all authors (up to 50) Copy
Kislyi V. P., Danilova E. B., Semenov V. V. Synthesis of isoxazolo[4,5-e][1,4]diazepin-5-ones from 5-acyl-4-(haloacetylamino)isoxazoles // Mendeleev Communications. 2012. Vol. 22. No. 2. pp. 85-86.
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TY - JOUR
DO - 10.1016/j.mencom.2012.03.011
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.03.011
TI - Synthesis of isoxazolo[4,5-e][1,4]diazepin-5-ones from 5-acyl-4-(haloacetylamino)isoxazoles
T2 - Mendeleev Communications
AU - Kislyi, Victor Petrovich
AU - Danilova, Evgenia Borisovna
AU - Semenov, Victor Vladimirovich
PY - 2012
DA - 2012/02/27
PB - Mendeleev Communications
SP - 85-86
IS - 2
VL - 22
ER -
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@article{2012_Kislyi,
author = {Victor Petrovich Kislyi and Evgenia Borisovna Danilova and Victor Vladimirovich Semenov},
title = {Synthesis of isoxazolo[4,5-e][1,4]diazepin-5-ones from 5-acyl-4-(haloacetylamino)isoxazoles},
journal = {Mendeleev Communications},
year = {2012},
volume = {22},
publisher = {Mendeleev Communications},
month = {Feb},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.03.011},
number = {2},
pages = {85--86},
doi = {10.1016/j.mencom.2012.03.011}
}
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Kislyi, Victor Petrovich, et al. “Synthesis of isoxazolo[4,5-e][1,4]diazepin-5-ones from 5-acyl-4-(haloacetylamino)isoxazoles.” Mendeleev Communications, vol. 22, no. 2, Feb. 2012, pp. 85-86. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.03.011.

Keywords

4-aminoisoxazole
basicity
isoxazolo[4,5-e][1,4]diazepin-5-one

Abstract

Treatment of 5-benzoyl-4-(iodoacetylamino)isoxazoles with alcoholic ammonia leads to isoxazolo[4,5-e][1,4]diazepin-5-ones, whereas the analogous chloroacetylamino derivatives are converted into a mixture of the deacylated 4-aminoisoxazoles and isoxazolo- [4,5-d]pyrimidines.

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