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Conjugated enynones: preparation, properties and applications in organic synthesis

Aleksander Aleksandrovich Golovanov 1
Aleksander Aleksandrovich Golovanov
, 
Ivan Sergeevich Odin 1
Ivan Sergeevich Odin
, 
Semen Solomonovich Zlotskii 2
Semen Solomonovich Zlotskii
1 Institute of Chemistry and Environmental Engineering, Togliatti State University, Russia
2 Ufa State Petroleum Technological University
10.1070/RCR4808
Published 30 November 2018
Review , RCR4808, Volume 88, Issue 3, 280-318
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Golovanov A. A., Odin I. S., Zlotskii S. S. Conjugated enynones: preparation, properties and applications in organic synthesis // Russian Chemical Reviews. 2018. Vol. 88. No. 3. pp. 280-318.
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Golovanov A. A., Odin I. S., Zlotskii S. S. Conjugated enynones: preparation, properties and applications in organic synthesis // Russian Chemical Reviews. 2018. Vol. 88. No. 3. pp. 280-318.
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TY - JOUR
DO - 10.1070/RCR4808
UR - https://rcr.colab.ws/publications/10.1070/RCR4808
TI - Conjugated enynones: preparation, properties and applications in organic synthesis
T2 - Russian Chemical Reviews
AU - Golovanov, Aleksander Aleksandrovich
AU - Odin, Ivan Sergeevich
AU - Zlotskii, Semen Solomonovich
PY - 2018
DA - 2018/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 280-318
IS - 3
VL - 88
ER -
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@article{2018_Golovanov,
author = {Aleksander Aleksandrovich Golovanov and Ivan Sergeevich Odin and Semen Solomonovich Zlotskii},
title = {Conjugated enynones: preparation, properties and applications in organic synthesis},
journal = {Russian Chemical Reviews},
year = {2018},
volume = {88},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RCR4808},
number = {3},
pages = {280--318},
doi = {10.1070/RCR4808}
}
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Golovanov, Aleksander Aleksandrovich, et al. “Conjugated enynones: preparation, properties and applications in organic synthesis.” Russian Chemical Reviews, vol. 88, no. 3, Nov. 2018, pp. 280-318. https://rcr.colab.ws/publications/10.1070/RCR4808.
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Abstract

Published data on the preparation methods, properties and chemical transformations of linear- and cross-conjugated enynones are integrated. The molecular and crystal structures, spectral characteristics and non-linear optical properties of these compounds are considered. Data on the reduction of enynones to alcohols and on electrophilic, nucleophilic and pericyclic reactions involving them are described systematically. Primary attention is paid to the regioselectivity and mechanisms of transformations of conjugated enynones. Examples of their application in the targeted organic synthesis of carbo- and heterocyclic compounds are given.

The bibliography includes 250 references.

Funders

Russian Science Foundation
18-13-00008

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