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Thermal isomerization of 3,3-dihalo-1,2-diphenylaziridines. / Kostikov, R. R.; Khlebnikov, A. F.; Ogloblin, K. A.

в: Chemistry of Heterocyclic Compounds, Том 14, № 1, 01.01.1978, стр. 37-41.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Kostikov, RR, Khlebnikov, AF & Ogloblin, KA 1978, 'Thermal isomerization of 3,3-dihalo-1,2-diphenylaziridines', Chemistry of Heterocyclic Compounds, Том. 14, № 1, стр. 37-41. https://doi.org/10.1007/BF00635939

APA

Vancouver

Kostikov RR, Khlebnikov AF, Ogloblin KA. Thermal isomerization of 3,3-dihalo-1,2-diphenylaziridines. Chemistry of Heterocyclic Compounds. 1978 Янв. 1;14(1):37-41. https://doi.org/10.1007/BF00635939

Author

Kostikov, R. R. ; Khlebnikov, A. F. ; Ogloblin, K. A. / Thermal isomerization of 3,3-dihalo-1,2-diphenylaziridines. в: Chemistry of Heterocyclic Compounds. 1978 ; Том 14, № 1. стр. 37-41.

BibTeX

@article{e983bab1c9f34e9192ce3a23cb4494ef,
title = "Thermal isomerization of 3,3-dihalo-1,2-diphenylaziridines",
abstract = "The kinetics of thermal isomerization of 3,3-dihalo-1,2-diphenylaziridines containing fluorine, chlorine, or bromine atoms in the ring were studied, and the activation parameters of the reaction were determined. A concerted mechanism for the formation of imidoyl halides from haloaziridines that includes conrotatory opening of the aziridine ring with halogen migration of the 1,2 type is proposed on the basis of the data obtained.",
author = "Kostikov, {R. R.} and Khlebnikov, {A. F.} and Ogloblin, {K. A.}",
year = "1978",
month = jan,
day = "1",
doi = "10.1007/BF00635939",
language = "English",
volume = "14",
pages = "37--41",
journal = "Chemistry of Heterocyclic Compounds",
issn = "0009-3122",
publisher = "Springer Nature",
number = "1",

}

RIS

TY - JOUR

T1 - Thermal isomerization of 3,3-dihalo-1,2-diphenylaziridines

AU - Kostikov, R. R.

AU - Khlebnikov, A. F.

AU - Ogloblin, K. A.

PY - 1978/1/1

Y1 - 1978/1/1

N2 - The kinetics of thermal isomerization of 3,3-dihalo-1,2-diphenylaziridines containing fluorine, chlorine, or bromine atoms in the ring were studied, and the activation parameters of the reaction were determined. A concerted mechanism for the formation of imidoyl halides from haloaziridines that includes conrotatory opening of the aziridine ring with halogen migration of the 1,2 type is proposed on the basis of the data obtained.

AB - The kinetics of thermal isomerization of 3,3-dihalo-1,2-diphenylaziridines containing fluorine, chlorine, or bromine atoms in the ring were studied, and the activation parameters of the reaction were determined. A concerted mechanism for the formation of imidoyl halides from haloaziridines that includes conrotatory opening of the aziridine ring with halogen migration of the 1,2 type is proposed on the basis of the data obtained.

UR - http://www.scopus.com/inward/record.url?scp=34250278924&partnerID=8YFLogxK

U2 - 10.1007/BF00635939

DO - 10.1007/BF00635939

M3 - Article

AN - SCOPUS:34250278924

VL - 14

SP - 37

EP - 41

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

SN - 0009-3122

IS - 1

ER -

ID: 28245228