том 80 издание 3 страницы 1375-1386

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

Тип публикацииJournal Article
Дата публикации2015-01-12
scimago Q2
wos Q1
БС1
SJR0.737
CiteScore6.1
Impact factor3.6
ISSN00223263, 15206904
Organic Chemistry
Краткое описание
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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ГОСТ |
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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.
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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.
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 -
BibTex |
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@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}
}
MLA
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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, vol. 80, no. 3, Jan. 2015, pp. 1375-1386. https://doi.org/10.1021/jo502135d.