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Chemistry of cross-conjugated dienones

, 
Aleksei Gennad'evich Golikov 2
Aleksei Gennad'evich Golikov
, 
Adel Pavlovna Kriven'ko 2
Adel Pavlovna Kriven'ko
, 
Nikolai Vasil'evich Zyk 1
Nikolai Vasil'evich Zyk
1 Lomonosov Moscow State University, Faculty of Chemistry
2 N. G. Chernyshevskii Saratov State University, Department of Chemistry
10.1070/RC2008v077n08ABEH003771
Published 30 November 2007
Communication , Volume 77, Issue 8, 661-681
45
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Vatsadze S. Z. et al. Chemistry of cross-conjugated dienones // Russian Chemical Reviews. 2008. Vol. 77. No. 8. pp. 661-681.
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Vatsadze S. Z., Golikov A. G., Kriven'ko A. P., Zyk N. V. Chemistry of cross-conjugated dienones // Russian Chemical Reviews. 2008. Vol. 77. No. 8. pp. 661-681.
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TY - JOUR
DO - 10.1070/RC2008v077n08ABEH003771
UR - https://rcr.colab.ws/publications/10.1070/RC2008v077n08ABEH003771
TI - Chemistry of cross-conjugated dienones
T2 - Russian Chemical Reviews
AU - Vatsadze, Sergey Zurabovich
AU - Golikov, Aleksei Gennad'evich
AU - Kriven'ko, Adel Pavlovna
AU - Zyk, Nikolai Vasil'evich
PY - 2008
DA - 2007/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 661-681
IS - 8
VL - 77
ER -
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@article{2008_Vatsadze,
author = {Sergey Zurabovich Vatsadze and Aleksei Gennad'evich Golikov and Adel Pavlovna Kriven'ko and Nikolai Vasil'evich Zyk},
title = {Chemistry of cross-conjugated dienones},
journal = {Russian Chemical Reviews},
year = {2008},
volume = {77},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC2008v077n08ABEH003771},
number = {8},
pages = {661--681},
doi = {10.1070/RC2008v077n08ABEH003771}
}
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Vatsadze, Sergey Zurabovich, et al. “Chemistry of cross-conjugated dienones.” Russian Chemical Reviews, vol. 77, no. 8, Nov. 2008, pp. 661-681. https://rcr.colab.ws/publications/10.1070/RC2008v077n08ABEH003771.
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Abstract

The review covers methods of synthesis, structure and properties of cross-conjugated dienones, viz., bis(arylmethylidene) derivatives of cyclic ketones and their heteroanalogues. The regio- and stereochemistry of the reactions of dienones depending on the ring size and the nature of substituents is analysed.