Azomethine ylides derived from dichlorocarbene and O-acylsalicylaldehyde anils in the synthesis of 2,5-epoxy-2,3,4,5-tetrahydro-1,4-benzoxazepin-2-ones and 2-aminoethanols

Standard

Azomethine ylides derived from dichlorocarbene and O-acylsalicylaldehyde anils in the synthesis of 2,5-epoxy-2,3,4,5-tetrahydro-1,4-benzoxazepin-2-ones and 2-aminoethanols. / Voznyi, I. V.; Novikov, M. S.; Khlebnikov, A. F.; Kostikov, R. R.

в: Russian Chemical Bulletin, Том 53, № 5, 05.2004, стр. 1087-1091.

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

BibTeX

@article{85f91d3c728c4e4ca049d9c2334ae299,

title = "Azomethine ylides derived from dichlorocarbene and O-acylsalicylaldehyde anils in the synthesis of 2,5-epoxy-2,3,4,5-tetrahydro-1,4-benzoxazepin-2-ones and 2-aminoethanols",

abstract = "Iminiodichloromethanides generated by the reaction of O-acylsalicylaldehyde anils with dichlorocarbene undergo regioselective intramolecular 1,3-dipolar cycloaddition to the ester carbonyl group to give 2,5-epoxy-2,3,4,5-tetrahydro- 1,4-benzoxazepin-2-ones. These compounds are expedient precursors for the synthesis of N-(2-hydroxybenzyl)ethanolamines.",

keywords = "aminoethanols, azomethine ylides, cycloaddition, dihalocarbenes",

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

note = "Funding Information: This study was financially supported by the Russian Foundation for Basic Research (Project No. 02 03 32735a) and the Ministry of Education of the Russian Federation (Project No. E02 5.0 30).",

year = "2004",

month = may,

doi = "10.1023/B:RUCB.0000041304.68814.83",

language = "English",

volume = "53",

pages = "1087--1091",

journal = "Russian Chemical Bulletin",

issn = "1066-5285",

publisher = "Springer Nature",

number = "5",

}

RIS

TY - JOUR

T1 - Azomethine ylides derived from dichlorocarbene and O-acylsalicylaldehyde anils in the synthesis of 2,5-epoxy-2,3,4,5-tetrahydro-1,4-benzoxazepin-2-ones and 2-aminoethanols

AU - Voznyi, I. V.

AU - Novikov, M. S.

AU - Khlebnikov, A. F.

AU - Kostikov, R. R.

N1 - Funding Information: This study was financially supported by the Russian Foundation for Basic Research (Project No. 02 03 32735a) and the Ministry of Education of the Russian Federation (Project No. E02 5.0 30).

PY - 2004/5

Y1 - 2004/5

N2 - Iminiodichloromethanides generated by the reaction of O-acylsalicylaldehyde anils with dichlorocarbene undergo regioselective intramolecular 1,3-dipolar cycloaddition to the ester carbonyl group to give 2,5-epoxy-2,3,4,5-tetrahydro- 1,4-benzoxazepin-2-ones. These compounds are expedient precursors for the synthesis of N-(2-hydroxybenzyl)ethanolamines.

AB - Iminiodichloromethanides generated by the reaction of O-acylsalicylaldehyde anils with dichlorocarbene undergo regioselective intramolecular 1,3-dipolar cycloaddition to the ester carbonyl group to give 2,5-epoxy-2,3,4,5-tetrahydro- 1,4-benzoxazepin-2-ones. These compounds are expedient precursors for the synthesis of N-(2-hydroxybenzyl)ethanolamines.

KW - aminoethanols

KW - azomethine ylides

KW - cycloaddition

KW - dihalocarbenes

UR - http://www.scopus.com/inward/record.url?scp=4544324176&partnerID=8YFLogxK

U2 - 10.1023/B:RUCB.0000041304.68814.83

DO - 10.1023/B:RUCB.0000041304.68814.83

M3 - Article

AN - SCOPUS:4544324176

VL - 53

SP - 1087

EP - 1091

JO - Russian Chemical Bulletin

JF - Russian Chemical Bulletin

SN - 1066-5285

IS - 5

ER -

ID: 99352466