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Acid-catalysed acylation of carbonyl compounds

Sergey Mikhaylovich Lukyanov 1
Sergey Mikhaylovich Lukyanov
, 
Alla Vasil'evna Koblik 1
Alla Vasil'evna Koblik
1 Institute of Physical and Organic Chemistry at Rostov State University
Published 30 November 1995
Communication , Volume 65, Issue 1, 1-25
7
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Lukyanov S. M., Koblik A. V. Acid-catalysed acylation of carbonyl compounds // Russian Chemical Reviews. 1996. Vol. 65. No. 1. pp. 1-25.
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Lukyanov S. M., Koblik A. V. Acid-catalysed acylation of carbonyl compounds // Russian Chemical Reviews. 1996. Vol. 65. No. 1. pp. 1-25.
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TY - JOUR
DO - 10.1070/RC1996v065n01ABEH000197
UR - https://rcr.colab.ws/publications/10.1070/RC1996v065n01ABEH000197
TI - Acid-catalysed acylation of carbonyl compounds
T2 - Russian Chemical Reviews
AU - Lukyanov, Sergey Mikhaylovich
AU - Koblik, Alla Vasil'evna
PY - 1996
DA - 1995/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 1-25
IS - 1
VL - 65
ER -
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@article{1996_Lukyanov,
author = {Sergey Mikhaylovich Lukyanov and Alla Vasil'evna Koblik},
title = {Acid-catalysed acylation of carbonyl compounds},
journal = {Russian Chemical Reviews},
year = {1996},
volume = {65},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC1996v065n01ABEH000197},
number = {1},
pages = {1--25},
doi = {10.1070/RC1996v065n01ABEH000197}
}
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Lukyanov, Sergey Mikhaylovich, and Alla Vasil'evna Koblik. “Acid-catalysed acylation of carbonyl compounds.” Russian Chemical Reviews, vol. 65, no. 1, Nov. 1996, pp. 1-25. https://rcr.colab.ws/publications/10.1070/RC1996v065n01ABEH000197.
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Abstract

Data concerning the O- and C-acylation of carbonyl compounds under acid catalysis conditions are surveyed. The properties of little-studied products of these reactions, i.e., acylals, α-haloalkyl acylates, and enol acylates are described. The acyloxycarbocations formed by acylation of aldehydes and ketones are characterised. The recently discovered new reactions of carbonyl compounds that lead to various heterocyclic and polyfunctional compounds are discussed.The bibliography includes 275 references.

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