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Push-pull enamines in the synthesis of fused azaheterocycles

Dmitry Viktorovich Dar’in 1
Dmitry Viktorovich Dar’in
, 
Pavel Sergeyevich Lobanov 1
Pavel Sergeyevich Lobanov
1 Institute of Chemistry, St. Petersburg State University
Published 30 November 2014
Communication , Volume 84, Issue 6, 601-633
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Dar’in D. V., Lobanov P. S. Push-pull enamines in the synthesis of fused azaheterocycles // Russian Chemical Reviews. 2015. Vol. 84. No. 6. pp. 601-633.
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Dar’in D. V., Lobanov P. S. Push-pull enamines in the synthesis of fused azaheterocycles // Russian Chemical Reviews. 2015. Vol. 84. No. 6. pp. 601-633.
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TY - JOUR
DO - 10.1070/RCR4528
UR - https://rcr.colab.ws/publications/10.1070/RCR4528
TI - Push-pull enamines in the synthesis of fused azaheterocycles
T2 - Russian Chemical Reviews
AU - Dar’in, Dmitry Viktorovich
AU - Lobanov, Pavel Sergeyevich
PY - 2015
DA - 2014/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 601-633
IS - 6
VL - 84
ER -
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@article{2015_Dar’in,
author = {Dmitry Viktorovich Dar’in and Pavel Sergeyevich Lobanov},
title = {Push-pull enamines in the synthesis of fused azaheterocycles},
journal = {Russian Chemical Reviews},
year = {2015},
volume = {84},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RCR4528},
number = {6},
pages = {601--633},
doi = {10.1070/RCR4528}
}
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Cite this
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Dar’in, Dmitry Viktorovich, and Pavel Sergeyevich Lobanov. “Push-pull enamines in the synthesis of fused azaheterocycles.” Russian Chemical Reviews, vol. 84, no. 6, Nov. 2015, pp. 601-633. https://rcr.colab.ws/publications/10.1070/RCR4528.
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Abstract

The review summarizes published data on the methods of the synthesis of fused nitrogen-containing heterocycles {\it via} push-pull enamines (mainly enaminones). Both intermolecular (cyclocondensations) and intramolecular (cyclizations) transformations of enamines, in which both nucleophilic centres of enamine (carbon and nitrogen) are incorporated into the resulting heterocycle, are considered. The data on the reactivity of enamines cover a~broad range of facile methods for the preparation of diverse fused pyridines (quinolines, isoquinolines, pyridopyridines, etc.) and pyrroles (indoles, tetrahydrocarbazoles, pyrrolopyridines,~etc.).

The bibliography includes 191 references.

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