Standard

1,3-Dipolar cycloaddition reactions of ketene imine ylides derived from dichlorocarbene and diphenylketene imines. / Novikov, M. S.; Khlebnikov, A. F.; Kostikov, R. R.

In: Russian Journal of Organic Chemistry, Vol. 32, No. 5, 01.05.1996, p. 637-644.

Research output: Contribution to journal › Article › peer-review

Harvard

Novikov, MS, Khlebnikov, AF & Kostikov, RR 1996, '1,3-Dipolar cycloaddition reactions of ketene imine ylides derived from dichlorocarbene and diphenylketene imines', Russian Journal of Organic Chemistry, vol. 32, no. 5, pp. 637-644.

APA

Novikov, M. S., Khlebnikov, A. F., & Kostikov, R. R. (1996). 1,3-Dipolar cycloaddition reactions of ketene imine ylides derived from dichlorocarbene and diphenylketene imines. Russian Journal of Organic Chemistry, 32(5), 637-644.

Vancouver

Novikov MS, Khlebnikov AF, Kostikov RR. 1,3-Dipolar cycloaddition reactions of ketene imine ylides derived from dichlorocarbene and diphenylketene imines. Russian Journal of Organic Chemistry. 1996 May 1;32(5):637-644.

Author

Novikov, M. S. ; Khlebnikov, A. F. ; Kostikov, R. R. / 1,3-Dipolar cycloaddition reactions of ketene imine ylides derived from dichlorocarbene and diphenylketene imines. In: Russian Journal of Organic Chemistry. 1996 ; Vol. 32, No. 5. pp. 637-644.

BibTeX

@article{70e065bc33254c53a655559be2334de6,
title = "1,3-Dipolar cycloaddition reactions of ketene imine ylides derived from dichlorocarbene and diphenylketene imines",
abstract = "Ketene imine ylides, generated from dichlorocarbene and diphenylketene alkyl- and arylimines undergo selective 1,3-dipolar cycloaddition to ethyl acrylate, methyl methacrylate, and acrylonitrile to give pyrrole and/or pyridine derivatives. The latter are formed by dichlorocyclopropanation of intermediate 2-chloropyrrolidones. A new type of transformation of ketene imine ylides to azomethine ylides was discovered in the reaction with methyl methacrylate.",
author = "Novikov, {M. S.} and Khlebnikov, {A. F.} and Kostikov, {R. R.}",
year = "1996",
month = may,
day = "1",
language = "English",
volume = "32",
pages = "637--644",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "5",

}

RIS

TY - JOUR

T1 - 1,3-Dipolar cycloaddition reactions of ketene imine ylides derived from dichlorocarbene and diphenylketene imines

AU - Novikov, M. S.

AU - Khlebnikov, A. F.

AU - Kostikov, R. R.

PY - 1996/5/1

Y1 - 1996/5/1

N2 - Ketene imine ylides, generated from dichlorocarbene and diphenylketene alkyl- and arylimines undergo selective 1,3-dipolar cycloaddition to ethyl acrylate, methyl methacrylate, and acrylonitrile to give pyrrole and/or pyridine derivatives. The latter are formed by dichlorocyclopropanation of intermediate 2-chloropyrrolidones. A new type of transformation of ketene imine ylides to azomethine ylides was discovered in the reaction with methyl methacrylate.

AB - Ketene imine ylides, generated from dichlorocarbene and diphenylketene alkyl- and arylimines undergo selective 1,3-dipolar cycloaddition to ethyl acrylate, methyl methacrylate, and acrylonitrile to give pyrrole and/or pyridine derivatives. The latter are formed by dichlorocyclopropanation of intermediate 2-chloropyrrolidones. A new type of transformation of ketene imine ylides to azomethine ylides was discovered in the reaction with methyl methacrylate.

UR - http://www.scopus.com/inward/record.url?scp=21544463028&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:21544463028

VL - 32

SP - 637

EP - 644

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 5

ER -

ID: 28246248