Intramolecular 1,3-dipolar cycloaddition to ester carbonyl of azomethinylides prepared from aldimines and difluorocarbene

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Intramolecular 1,3-dipolar cycloaddition to ester carbonyl of azomethinylides prepared from aldimines and difluorocarbene. / Voznyi, I. V.; Novikov, M. S.; Khlebnikov, A. F.; Kopf, J.; Kostikov, R. R.

в: Russian Journal of Organic Chemistry, Том 40, № 2, 02.2004, стр. 199-205.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

BibTeX

@article{4929af08beca4132bf3feb41765ee668,

title = "Intramolecular 1,3-dipolar cycloaddition to ester carbonyl of azomethinylides prepared from aldimines and difluorocarbene",

abstract = "Azomethinylides generated by reaction of difluorocarbene with N-alkyl- and N-arylimines of O-acylated salycilaldehyde undergo intramolecular 1,3-dipolar cycloaddition to the ester carbonyl group forming regioselectively 2,5-epoxy-1,4-benzoxazepine derivatives.",

author = "Voznyi, {I. V.} and Novikov, {M. S.} and Khlebnikov, {A. F.} and J. Kopf and Kostikov, {R. R.}",

note = "Funding Information: The study was carried out under financial support of the Russian Foundation for Basic Research (grant 02- 03-32735a), of the Ministry of Education of the Russian Federation (grant E02-5.0-30), and INTAS program (grant 00-0549).",

year = "2004",

month = feb,

doi = "10.1023/B:RUJO.0000034942.42778.e0",

language = "English",

volume = "40",

pages = "199--205",

journal = "Russian Journal of Organic Chemistry",

issn = "1070-4280",

publisher = "МАИК {"}Наука/Интерпериодика{"}",

number = "2",

}

RIS

TY - JOUR

T1 - Intramolecular 1,3-dipolar cycloaddition to ester carbonyl of azomethinylides prepared from aldimines and difluorocarbene

AU - Voznyi, I. V.

AU - Novikov, M. S.

AU - Khlebnikov, A. F.

AU - Kopf, J.

AU - Kostikov, R. R.

N1 - Funding Information: The study was carried out under financial support of the Russian Foundation for Basic Research (grant 02- 03-32735a), of the Ministry of Education of the Russian Federation (grant E02-5.0-30), and INTAS program (grant 00-0549).

PY - 2004/2

Y1 - 2004/2

N2 - Azomethinylides generated by reaction of difluorocarbene with N-alkyl- and N-arylimines of O-acylated salycilaldehyde undergo intramolecular 1,3-dipolar cycloaddition to the ester carbonyl group forming regioselectively 2,5-epoxy-1,4-benzoxazepine derivatives.

AB - Azomethinylides generated by reaction of difluorocarbene with N-alkyl- and N-arylimines of O-acylated salycilaldehyde undergo intramolecular 1,3-dipolar cycloaddition to the ester carbonyl group forming regioselectively 2,5-epoxy-1,4-benzoxazepine derivatives.

UR - http://www.scopus.com/inward/record.url?scp=3542999263&partnerID=8YFLogxK

U2 - 10.1023/B:RUJO.0000034942.42778.e0

DO - 10.1023/B:RUJO.0000034942.42778.e0

M3 - Article

VL - 40

SP - 199

EP - 205

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 2

ER -

ID: 5029295