Open Access
A novel acid-catalyzed rearrangement of 2-substituted-3-(2-nitrophenyl)oxiranes for the synthesis of di- and mono-oxalamides
V. A. Mamedov
1, 2
,
Vera L Mamedova
1, 2
,
Gulnas Z Khikmatova
2
,
E. V. Mironova
1
,
Dmitry B. Krivolapov
1
,
Olga B Bazanova
1
,
D.V. Chachkov
2
,
Publication type: Journal Article
Publication date: 2016-03-11
scimago Q1
wos Q2
SJR: 0.777
CiteScore: 7.6
Impact factor: 4.6
ISSN: 20462069
General Chemistry
General Chemical Engineering
Abstract
A novel one-pot synthetic approach to N1-(2-carboxyaryl)-N2-(aryl or H)oxalamides from 3-(2-nitroaryl)oxirane-2-carboxamides via the classical Meinwald rearrangement and a new rearrangement sequence has been developed. The methodology is applicable to the synthesis of N-(2-carboxyphenyl)aryloxalmonoamides from (3-(2-nitrophenyl)oxiran-2-yl)(aryl)methanones. The method is operationally simple and high yielding, thus providing a new useful formula for both anthranilic acid derivatives and oxalamides.
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Total citations:
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Citations from 2024:
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(20.83%)
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GOST
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Mamedov V. A. et al. A novel acid-catalyzed rearrangement of 2-substituted-3-(2-nitrophenyl)oxiranes for the synthesis of di- and mono-oxalamides // RSC Advances. 2016. Vol. 6. No. 33. pp. 27885-27895.
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Mamedov V. A., Mamedova V. L., Khikmatova G. Z., Mironova E. V., Krivolapov D. B., Bazanova O. B., Chachkov D., Katsyuba S. A., Rizvanov I. Kh., Latypov S. A novel acid-catalyzed rearrangement of 2-substituted-3-(2-nitrophenyl)oxiranes for the synthesis of di- and mono-oxalamides // RSC Advances. 2016. Vol. 6. No. 33. pp. 27885-27895.
Cite this
RIS
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TY - JOUR
DO - 10.1039/C6RA02586B
UR - https://doi.org/10.1039/C6RA02586B
TI - A novel acid-catalyzed rearrangement of 2-substituted-3-(2-nitrophenyl)oxiranes for the synthesis of di- and mono-oxalamides
T2 - RSC Advances
AU - Mamedov, V. A.
AU - Mamedova, Vera L
AU - Khikmatova, Gulnas Z
AU - Mironova, E. V.
AU - Krivolapov, Dmitry B.
AU - Bazanova, Olga B
AU - Chachkov, D.V.
AU - Katsyuba, Sergey A.
AU - Rizvanov, Ildar Kh
AU - Latypov, Shamil
PY - 2016
DA - 2016/03/11
PB - Royal Society of Chemistry (RSC)
SP - 27885-27895
IS - 33
VL - 6
SN - 2046-2069
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2016_Mamedov,
author = {V. A. Mamedov and Vera L Mamedova and Gulnas Z Khikmatova and E. V. Mironova and Dmitry B. Krivolapov and Olga B Bazanova and D.V. Chachkov and Sergey A. Katsyuba and Ildar Kh Rizvanov and Shamil Latypov},
title = {A novel acid-catalyzed rearrangement of 2-substituted-3-(2-nitrophenyl)oxiranes for the synthesis of di- and mono-oxalamides},
journal = {RSC Advances},
year = {2016},
volume = {6},
publisher = {Royal Society of Chemistry (RSC)},
month = {mar},
url = {https://doi.org/10.1039/C6RA02586B},
number = {33},
pages = {27885--27895},
doi = {10.1039/C6RA02586B}
}
Cite this
MLA
Copy
Mamedov, V. A., et al. “A novel acid-catalyzed rearrangement of 2-substituted-3-(2-nitrophenyl)oxiranes for the synthesis of di- and mono-oxalamides.” RSC Advances, vol. 6, no. 33, Mar. 2016, pp. 27885-27895. https://doi.org/10.1039/C6RA02586B.