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Pyrido- and pyrimidoisoindoles: methods of synthesis and properties

A A Pokholenko 1
A A Pokholenko
, 
Zoya Vsevolodovna Voitenko 1
Zoya Vsevolodovna Voitenko
, 
Vladimir Alekseevich Kovtunenko 1
Vladimir Alekseevich Kovtunenko
1 National Taras Shevchenko University of Kyiv, Chemical Faculty
Published 30 November 2003
Communication , Volume 73, Issue 8, 771-784
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Pokholenko A. A., Voitenko Z. V., Kovtunenko V. A. Pyrido- and pyrimidoisoindoles: methods of synthesis and properties // Russian Chemical Reviews. 2004. Vol. 73. No. 8. pp. 771-784.
GOST all authors (up to 50)
Pokholenko A. A., Voitenko Z. V., Kovtunenko V. A. Pyrido- and pyrimidoisoindoles: methods of synthesis and properties // Russian Chemical Reviews. 2004. Vol. 73. No. 8. pp. 771-784.
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TY - JOUR
DO - 10.1070/RC2004v073n08ABEH000906
UR - https://rcr.colab.ws/publications/10.1070/RC2004v073n08ABEH000906
TI - Pyrido- and pyrimidoisoindoles: methods of synthesis and properties
T2 - Russian Chemical Reviews
AU - Pokholenko, A A
AU - Voitenko, Zoya Vsevolodovna
AU - Kovtunenko, Vladimir Alekseevich
PY - 2004
DA - 2003/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 771-784
IS - 8
VL - 73
ER -
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@article{2004_Pokholenko,
author = {A A Pokholenko and Zoya Vsevolodovna Voitenko and Vladimir Alekseevich Kovtunenko},
title = {Pyrido- and pyrimidoisoindoles: methods of synthesis and properties},
journal = {Russian Chemical Reviews},
year = {2004},
volume = {73},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC2004v073n08ABEH000906},
number = {8},
pages = {771--784},
doi = {10.1070/RC2004v073n08ABEH000906}
}
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Pokholenko, A. A., et al. “Pyrido- and pyrimidoisoindoles: methods of synthesis and properties.” Russian Chemical Reviews, vol. 73, no. 8, Nov. 2004, pp. 771-784. https://rcr.colab.ws/publications/10.1070/RC2004v073n08ABEH000906.
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Abstract

The data on the synthesis, structures and chemical properties of pyrido- and pyrimidoisoindole derivatives with an azine ring annelated to a pyrrole ring, which have been published over the last two decades, are generalised. The structure of the π-electron system and the high reactivities of azinoisoindoles are discussed. Special attention is given to aromatic pyrido- and pyrimidoisoindoles.