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Synthesis of 5-aminoisoxazoles from 3-trimethylsilylprop-2-ynamides

Mikhail Victorovich Andreev 1
Mikhail Victorovich Andreev
, 
Alevtina Sergeevna Medvedeva 1
Alevtina Sergeevna Medvedeva
, 
Lyudmila Ivanovna Larina 1
Lyudmila Ivanovna Larina
, 
Maria Matveevna Demina 1
Maria Matveevna Demina
10.1016/j.mencom.2017.03.023
Published 2017-02-27
Communication , Volume 27, Issue 2, 175-177
20
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Andreev M. V. et al. Synthesis of 5-aminoisoxazoles from 3-trimethylsilylprop-2-ynamides // Mendeleev Communications. 2017. Vol. 27. No. 2. pp. 175-177.
GOST all authors (up to 50) Copy
Andreev M. V., Medvedeva A. S., Larina L. I., Demina M. M. Synthesis of 5-aminoisoxazoles from 3-trimethylsilylprop-2-ynamides // Mendeleev Communications. 2017. Vol. 27. No. 2. pp. 175-177.
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TY - JOUR
DO - 10.1016/j.mencom.2017.03.023
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.03.023
TI - Synthesis of 5-aminoisoxazoles from 3-trimethylsilylprop-2-ynamides
T2 - Mendeleev Communications
AU - Andreev, Mikhail Victorovich
AU - Medvedeva, Alevtina Sergeevna
AU - Larina, Lyudmila Ivanovna
AU - Demina, Maria Matveevna
PY - 2017
DA - 2017/02/27
PB - Mendeleev Communications
SP - 175-177
IS - 2
VL - 27
ER -
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@article{2017_Andreev,
author = {Mikhail Victorovich Andreev and Alevtina Sergeevna Medvedeva and Lyudmila Ivanovna Larina and Maria Matveevna Demina},
title = {Synthesis of 5-aminoisoxazoles from 3-trimethylsilylprop-2-ynamides},
journal = {Mendeleev Communications},
year = {2017},
volume = {27},
publisher = {Mendeleev Communications},
month = {Feb},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.03.023},
number = {2},
pages = {175--177},
doi = {10.1016/j.mencom.2017.03.023}
}
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Cite this
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Andreev, Mikhail Victorovich, et al. “Synthesis of 5-aminoisoxazoles from 3-trimethylsilylprop-2-ynamides.” Mendeleev Communications, vol. 27, no. 2, Feb. 2017, pp. 175-177. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.03.023.

Abstract

Reaction between N,N-disubstituted 3-trimethylsilylprop-2-ynamides and ammonium azide under mild conditions affords hitherto unknown 5-aminoisoxazole derivatives in good yields.

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