Rearrangement of Quinoxalin-2-ones When Exposed to Enamines Generated in Situ from Ketones and Ammonium Acetate: Method for the Synthesis of 1-(Pyrrolyl)benzimidazolones
V. A. Mamedov
1, 2
,
Nataliya A Zhukova
1, 2
,
Tatyana N Beschastnova
1
,
Dmitry B. Krivolapov
1
,
E. V. Mironova
1
,
Anastasiya I Zamaletdinova
2
,
Publication type: Journal Article
Publication date: 2015-01-12
scimago Q2
wos Q1
SJR: 0.737
CiteScore: 6.1
Impact factor: 3.6
ISSN: 00223263, 15206904
PubMed ID:
25496019
Organic Chemistry
Abstract
The reaction of 3-benzoylquinoxalin-2(1H)-ones with enamines (generated in situ from ammonium acetate and the corresponding methylaryl(hetaryl)ketones) proceeds smoothly to give the corresponding substituted 1-(pyrrolyl)benzimidazolone derivatives in moderate yields through the novel rearrangement of 3-benzoylquinoxalin-2(1H)-ones involving a dual cleavage of the C3═N4 and C2-C3 bonds under mild conditions.
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Total citations:
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Citations from 2024:
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GOST
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Mamedov V. A. et al. Rearrangement of Quinoxalin-2-ones When Exposed to Enamines Generated in Situ from Ketones and Ammonium Acetate: Method for the Synthesis of 1-(Pyrrolyl)benzimidazolones // Journal of Organic Chemistry. 2015. Vol. 80. No. 3. pp. 1375-1386.
GOST all authors (up to 50)
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Mamedov V. A., Zhukova N. A., Beschastnova T. N., Syakaev V. V., Krivolapov D. B., Mironova E. V., Zamaletdinova A. I., Rizvanov I. Kh., Latypov S. Rearrangement of Quinoxalin-2-ones When Exposed to Enamines Generated in Situ from Ketones and Ammonium Acetate: Method for the Synthesis of 1-(Pyrrolyl)benzimidazolones // Journal of Organic Chemistry. 2015. Vol. 80. No. 3. pp. 1375-1386.
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RIS
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TY - JOUR
DO - 10.1021/jo502135d
UR - https://doi.org/10.1021/jo502135d
TI - Rearrangement of Quinoxalin-2-ones When Exposed to Enamines Generated in Situ from Ketones and Ammonium Acetate: Method for the Synthesis of 1-(Pyrrolyl)benzimidazolones
T2 - Journal of Organic Chemistry
AU - Mamedov, V. A.
AU - Zhukova, Nataliya A
AU - Beschastnova, Tatyana N
AU - Syakaev, Victor V.
AU - Krivolapov, Dmitry B.
AU - Mironova, E. V.
AU - Zamaletdinova, Anastasiya I
AU - Rizvanov, Ildar Kh
AU - Latypov, Shamil
PY - 2015
DA - 2015/01/12
PB - American Chemical Society (ACS)
SP - 1375-1386
IS - 3
VL - 80
PMID - 25496019
SN - 0022-3263
SN - 1520-6904
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2015_Mamedov,
author = {V. A. Mamedov and Nataliya A Zhukova and Tatyana N Beschastnova and Victor V. Syakaev and Dmitry B. Krivolapov and E. V. Mironova and Anastasiya I Zamaletdinova and Ildar Kh Rizvanov and Shamil Latypov},
title = {Rearrangement of Quinoxalin-2-ones When Exposed to Enamines Generated in Situ from Ketones and Ammonium Acetate: Method for the Synthesis of 1-(Pyrrolyl)benzimidazolones},
journal = {Journal of Organic Chemistry},
year = {2015},
volume = {80},
publisher = {American Chemical Society (ACS)},
month = {jan},
url = {https://doi.org/10.1021/jo502135d},
number = {3},
pages = {1375--1386},
doi = {10.1021/jo502135d}
}
Cite this
MLA
Copy
Mamedov, V. A., et al. “Rearrangement of Quinoxalin-2-ones When Exposed to Enamines Generated in Situ from Ketones and Ammonium Acetate: Method for the Synthesis of 1-(Pyrrolyl)benzimidazolones.” Journal of Organic Chemistry, vol. 80, no. 3, Jan. 2015, pp. 1375-1386. https://doi.org/10.1021/jo502135d.