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Electrophilic Amination

È Schmitz 1
È Schmitz
1 Central Institute of Organic Chemistry of the Academy of Sciences of the GDR
10.1070/RC1976v045n01ABEH002586
Published 30 November 1975
Communication , Volume 45, Issue 1, 16-24
20
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Schmitz È. Electrophilic Amination // Russian Chemical Reviews. 1976. Vol. 45. No. 1. pp. 16-24.
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Schmitz È. Electrophilic Amination // Russian Chemical Reviews. 1976. Vol. 45. No. 1. pp. 16-24.
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TY - JOUR
DO - 10.1070/RC1976v045n01ABEH002586
UR - https://rcr.colab.ws/publications/10.1070/RC1976v045n01ABEH002586
TI - Electrophilic Amination
T2 - Russian Chemical Reviews
AU - Schmitz, È
PY - 1976
DA - 1975/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 16-24
IS - 1
VL - 45
ER -
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@article{1976_Schmitz,
author = {È Schmitz},
title = {Electrophilic Amination},
journal = {Russian Chemical Reviews},
year = {1976},
volume = {45},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC1976v045n01ABEH002586},
number = {1},
pages = {16--24},
doi = {10.1070/RC1976v045n01ABEH002586}
}
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Schmitz, È.. “Electrophilic Amination.” Russian Chemical Reviews, vol. 45, no. 1, Nov. 1976, pp. 16-24. https://rcr.colab.ws/publications/10.1070/RC1976v045n01ABEH002586.
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Abstract

The review is devoted to reactions in which amino-, alkylamino- and acylamino-groups are transferred to nucleophilic agents. Electrophilic aminating agents are chloramine, hydroxylamine-O-sulphonic acid, oxaziridines unsubstituted at the nitrogen atom, and N-acyloxaziridines. The formation of three-membered rings with two heteroatoms, occurring as intramolecular electrophilic amination, is discussed.
The bibliography includes 99 references.