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The progress in the chemistry of N-acyliminium ions and their use in stereoselective organic synthesis

Maksim Gavrilovich Vinogradov 1
Maksim Gavrilovich Vinogradov
, 
Olga Vasil'evna Turova 1
Olga Vasil'evna Turova
, 
Sergei Grigorievich Zlotin 1
Sergei Grigorievich Zlotin
1 N.D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences
Published 30 November 2016
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Vinogradov M. G., Turova O. V., Zlotin S. G. The progress in the chemistry of N-acyliminium ions and their use in stereoselective organic synthesis // Russian Chemical Reviews. 2016. Vol. 86. No. 1. pp. 1-17.
GOST all authors (up to 50)
Vinogradov M. G., Turova O. V., Zlotin S. G. The progress in the chemistry of N-acyliminium ions and their use in stereoselective organic synthesis // Russian Chemical Reviews. 2016. Vol. 86. No. 1. pp. 1-17.
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TY - JOUR
DO - 10.1070/RCR4628
UR - https://rcr.colab.ws/publications/10.1070/RCR4628
TI - The progress in the chemistry of N-acyliminium ions and their use in stereoselective organic synthesis
T2 - Russian Chemical Reviews
AU - Vinogradov, Maksim Gavrilovich
AU - Turova, Olga Vasil'evna
AU - Zlotin, Sergei Grigorievich
PY - 2016
DA - 2016/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 1-17
IS - 1
VL - 86
ER -
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@article{2016_Vinogradov,
author = {Maksim Gavrilovich Vinogradov and Olga Vasil'evna Turova and Sergei Grigorievich Zlotin},
title = {The progress in the chemistry of N-acyliminium ions and their use in stereoselective organic synthesis},
journal = {Russian Chemical Reviews},
year = {2016},
volume = {86},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RCR4628},
number = {1},
pages = {1--17},
doi = {10.1070/RCR4628}
}
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Vinogradov, Maksim Gavrilovich, et al. “The progress in the chemistry of N-acyliminium ions and their use in stereoselective organic synthesis.” Russian Chemical Reviews, vol. 86, no. 1, Nov. 2016, pp. 1-17. https://rcr.colab.ws/publications/10.1070/RCR4628.
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Abstract

The review summarizes data published in the last decade on the reactions of organic compounds involving N-acyliminium ions, including intramolecular arylation (cyclization), cross-coupling with nucleophiles and some other transformations to form new carbon--carbon and carbon--heteroatom bonds. The stereo- and enantioselective versions of these reactions using chiral auxiliaries and asymmetric catalysts (organocatalysts) are considered. Examples of application of N-acyliminium ions for the synthesis of natural compounds and their analogues are presented.

The bibliography includes 100 references.

Funders

Russian Science Foundation
14-50-00126