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The Electronic and Steric Effects in Heterolytic Intramolecular Cyclisation Reactions

Raymond Èduardovich Valters 1
Raymond Èduardovich Valters
1 Riga Technical University
10.1070/RC1982v051n08ABEH002911
Published 30 November 1981
Communication , Volume 51, Issue 8, 788-801
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Valters R. È. The Electronic and Steric Effects in Heterolytic Intramolecular Cyclisation Reactions // Russian Chemical Reviews. 1982. Vol. 51. No. 8. pp. 788-801.
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Valters R. È. The Electronic and Steric Effects in Heterolytic Intramolecular Cyclisation Reactions // Russian Chemical Reviews. 1982. Vol. 51. No. 8. pp. 788-801.
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TY - JOUR
DO - 10.1070/RC1982v051n08ABEH002911
UR - https://rcr.colab.ws/publications/10.1070/RC1982v051n08ABEH002911
TI - The Electronic and Steric Effects in Heterolytic Intramolecular Cyclisation Reactions
T2 - Russian Chemical Reviews
AU - Valters, Raymond Èduardovich
PY - 1982
DA - 1981/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 788-801
IS - 8
VL - 51
ER -
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@article{1982_Valters,
author = {Raymond Èduardovich Valters},
title = {The Electronic and Steric Effects in Heterolytic Intramolecular Cyclisation Reactions},
journal = {Russian Chemical Reviews},
year = {1982},
volume = {51},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC1982v051n08ABEH002911},
number = {8},
pages = {788--801},
doi = {10.1070/RC1982v051n08ABEH002911}
}
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Valters, Raymond Èduardovich. “The Electronic and Steric Effects in Heterolytic Intramolecular Cyclisation Reactions.” Russian Chemical Reviews, vol. 51, no. 8, Nov. 1982, pp. 788-801. https://rcr.colab.ws/publications/10.1070/RC1982v051n08ABEH002911.
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Abstract

Data concerning the influence of the electronic and steric effects of substituents as well as the structure of the connecting units on the rate and equilibrium constants for cyclisation reactions, occurring as intramolecular nucleophilic addition to a trigonal carbon atom, are examined. The general characteristics permitting the prediction of the ease of ring closure and the stability of the heterocycles are specified.
The bibliography includes 166 references.