Tandem double acylation/[3,3]-rearrangement of aliphatic nitro compounds: a route to α-oxygenated oxime derivatives
Yulia A Antonova
1, 2, 3, 4, 5, 6, 7
,
Yulia V. Nelyubina
4, 5, 6, 8, 9
,
Alexey Yu Sukhorukov
1, 3, 4, 5, 6
,
Sema L. Ioffe
1, 3, 4, 5, 6
,
Andrey A Tabolin
1, 3, 4, 5, 6
4
RUSSIAN ACADEMY OF SCIENCES
5
Moscow
6
RUSSIAN FEDERATION
|
7
DEPARTMENT OF CHEMISTRY
Publication type: Journal Article
Publication date: 2019-05-29
scimago Q2
wos Q2
SJR: 0.600
CiteScore: 5.2
Impact factor: 2.7
ISSN: 14770520, 14770539
PubMed ID:
31166349
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
A new tandem double acylation/rearrangement reaction of nitro compounds is described. It has a broad substrate scope allowing the mild and efficient synthesis of α-acyloxy oxime esters in high yields and regioselectivity. According to the obtained data, the mechanism for transformation was proposed. The utility of the obtained α-hydroxy oxime esters was demonstrated.
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Total citations:
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Citations from 2024:
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Antonova Y. A. et al. Tandem double acylation/[3,3]-rearrangement of aliphatic nitro compounds: a route to α-oxygenated oxime derivatives // Organic and Biomolecular Chemistry. 2019. Vol. 17. No. 24. pp. 5997-6006.
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Antonova Y. A., Nelyubina Y. V., Sukhorukov A. Yu., Ioffe S. L., Tabolin A. A. Tandem double acylation/[3,3]-rearrangement of aliphatic nitro compounds: a route to α-oxygenated oxime derivatives // Organic and Biomolecular Chemistry. 2019. Vol. 17. No. 24. pp. 5997-6006.
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RIS
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TY - JOUR
DO - 10.1039/c9ob01005j
UR - https://xlink.rsc.org/?DOI=C9OB01005J
TI - Tandem double acylation/[3,3]-rearrangement of aliphatic nitro compounds: a route to α-oxygenated oxime derivatives
T2 - Organic and Biomolecular Chemistry
AU - Antonova, Yulia A
AU - Nelyubina, Yulia V.
AU - Sukhorukov, Alexey Yu
AU - Ioffe, Sema L.
AU - Tabolin, Andrey A
PY - 2019
DA - 2019/05/29
PB - Royal Society of Chemistry (RSC)
SP - 5997-6006
IS - 24
VL - 17
PMID - 31166349
SN - 1477-0520
SN - 1477-0539
ER -
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@article{2019_Antonova,
author = {Yulia A Antonova and Yulia V. Nelyubina and Alexey Yu Sukhorukov and Sema L. Ioffe and Andrey A Tabolin},
title = {Tandem double acylation/[3,3]-rearrangement of aliphatic nitro compounds: a route to α-oxygenated oxime derivatives},
journal = {Organic and Biomolecular Chemistry},
year = {2019},
volume = {17},
publisher = {Royal Society of Chemistry (RSC)},
month = {may},
url = {https://xlink.rsc.org/?DOI=C9OB01005J},
number = {24},
pages = {5997--6006},
doi = {10.1039/c9ob01005j}
}
Cite this
MLA
Copy
Antonova, Yulia A., et al. “Tandem double acylation/[3,3]-rearrangement of aliphatic nitro compounds: a route to α-oxygenated oxime derivatives.” Organic and Biomolecular Chemistry, vol. 17, no. 24, May. 2019, pp. 5997-6006. https://xlink.rsc.org/?DOI=C9OB01005J.