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The chemistry of acetylcyclopropane

Boris Arnol'dovich Cheskis 1
Boris Arnol'dovich Cheskis
, 
Natalya M Ivanova 2
Natalya M Ivanova
, 
Aiexsander Makarovich Moiseenkov 1
Aiexsander Makarovich Moiseenkov
, 
Oleg Matveevich Nefedov 1
Oleg Matveevich Nefedov
1 N. D. Zelinskii Institute of Organic Chemistry, Moscow
2 Joint-Stock Company "Kaprolactam", Dzerzhinsk, Nizhegorodskii Region
10.1070/RC1993v062n04ABEH000021
Published 30 November 1992
Communication , Volume 62, Issue 4, 337-358
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Cheskis B. A. et al. The chemistry of acetylcyclopropane // Russian Chemical Reviews. 1993. Vol. 62. No. 4. pp. 337-358.
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Cheskis B. A., Ivanova N. M., Moiseenkov A. M., Nefedov O. M. The chemistry of acetylcyclopropane // Russian Chemical Reviews. 1993. Vol. 62. No. 4. pp. 337-358.
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TY - JOUR
DO - 10.1070/RC1993v062n04ABEH000021
UR - https://rcr.colab.ws/publications/10.1070/RC1993v062n04ABEH000021
TI - The chemistry of acetylcyclopropane
T2 - Russian Chemical Reviews
AU - Cheskis, Boris Arnol'dovich
AU - Ivanova, Natalya M
AU - Moiseenkov, Aiexsander Makarovich
AU - Nefedov, Oleg Matveevich
PY - 1993
DA - 1992/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 337-358
IS - 4
VL - 62
ER -
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@article{1993_Cheskis,
author = {Boris Arnol'dovich Cheskis and Natalya M Ivanova and Aiexsander Makarovich Moiseenkov and Oleg Matveevich Nefedov},
title = {The chemistry of acetylcyclopropane},
journal = {Russian Chemical Reviews},
year = {1993},
volume = {62},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC1993v062n04ABEH000021},
number = {4},
pages = {337--358},
doi = {10.1070/RC1993v062n04ABEH000021}
}
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Cheskis, Boris Arnol'dovich, et al. “The chemistry of acetylcyclopropane.” Russian Chemical Reviews, vol. 62, no. 4, Nov. 1993, pp. 337-358. https://rcr.colab.ws/publications/10.1070/RC1993v062n04ABEH000021.
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Abstract

Data on the synthesis chemical reactions of acetylcyclopropane are presented. A systematic account is given in terms of the reactions of the functional groups of the above compound (methyl, carbonyl, and cyclopropyl). The extensive possibilities of acetylcyclopropane as a convenient five-carbon building block in organic synthesis are demonstrated. The bibliography includes 268 references.

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