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Rearrangement of 3-aminoisoxazolo[4,5-c]coumarins into 2-aminooxazolo[4,5-c]coumarins mediated by carboxylic acid anhydrides

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Sosnovskikh V. Y., Moshkin V. S., Kodess M. I. Rearrangement of 3-aminoisoxazolo[4,5-c]coumarins into 2-aminooxazolo[4,5-c]coumarins mediated by carboxylic acid anhydrides // Mendeleev Communications. 2010. Vol. 20. No. 4. pp. 209-211.
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Sosnovskikh V. Y., Moshkin V. S., Kodess M. I. Rearrangement of 3-aminoisoxazolo[4,5-c]coumarins into 2-aminooxazolo[4,5-c]coumarins mediated by carboxylic acid anhydrides // Mendeleev Communications. 2010. Vol. 20. No. 4. pp. 209-211.
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TY - JOUR
DO - 10.1016/j.mencom.2010.06.009
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2010.06.009
TI - Rearrangement of 3-aminoisoxazolo[4,5-c]coumarins into 2-aminooxazolo[4,5-c]coumarins mediated by carboxylic acid anhydrides
T2 - Mendeleev Communications
AU - Sosnovskikh, Vyacheslav Yakovlevich
AU - Moshkin, Vladimir Sergeevich
AU - Kodess, Mikhail Isaakovich
PY - 2010
DA - 2010/06/16
PB - Mendeleev Communications
SP - 209-211
IS - 4
VL - 20
ER -
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@article{2010_Sosnovskikh,
author = {Vyacheslav Yakovlevich Sosnovskikh and Vladimir Sergeevich Moshkin and Mikhail Isaakovich Kodess},
title = {Rearrangement of 3-aminoisoxazolo[4,5-c]coumarins into 2-aminooxazolo[4,5-c]coumarins mediated by carboxylic acid anhydrides},
journal = {Mendeleev Communications},
year = {2010},
volume = {20},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2010.06.009},
number = {4},
pages = {209--211},
doi = {10.1016/j.mencom.2010.06.009}
}
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Sosnovskikh, Vyacheslav Yakovlevich, et al. “Rearrangement of 3-aminoisoxazolo[4,5-c]coumarins into 2-aminooxazolo[4,5-c]coumarins mediated by carboxylic acid anhydrides.” Mendeleev Communications, vol. 20, no. 4, Jun. 2010, pp. 209-211. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2010.06.009.

Abstract

Reactions of 3-amino-4H-chromeno[3,4-d]isoxazol-4-ones with acetic and trifluoroacetic anhydrides gave the corresponding acetyl derivatives, which were rearranged into 2-amino-4H-chromeno[3,4-d][1,3]oxazol-4-ones by heating in DMSO solution.

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