2-(aminoaryl)alkanone O-phenyl oximes: versatile reagents for syntheses of quinazolines

Fernando Portela-Cubillo; Jackie S. Scott; John C. Walton

doi:10.1039/b803630f

2-(aminoaryl)alkanone O-phenyl oximes: versatile reagents for syntheses of quinazolines

Fernando Portela-Cubillo
, Jackie S. Scott
, John C. Walton

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

Abstract

Microwave irradiations of 2-(aminoaryl)alkanone O-phenyl oximes and carbonyl compounds generate iminyl radicals in company with imines; iminyl on imine ring closure yields dihydroquinazolines or quinazolines when ZnCl2 is included in the mixture.

Original language	English
Pages (from-to)	2935-2937
Number of pages	3
Journal	Chemical Communications
Issue number	25
DOIs	https://doi.org/10.1039/b803630f
Publication status	Published - 2008

Keywords

RADICAL CYCLIZATION
IMINYL RADICALS
INHIBITORS
ACETYLOXIMES
DERIVATIVES
PYRIDINES
ACETONE
AGENTS

Access to Document

10.1039/b803630f

Handle.net

Persistent link

Cite this

@article{b31f000e311e48868d2969b6edf857fa,

title = "2-(aminoaryl)alkanone O-phenyl oximes: versatile reagents for syntheses of quinazolines",

abstract = "Microwave irradiations of 2-(aminoaryl)alkanone O-phenyl oximes and carbonyl compounds generate iminyl radicals in company with imines; iminyl on imine ring closure yields dihydroquinazolines or quinazolines when ZnCl2 is included in the mixture.",

keywords = "RADICAL CYCLIZATION, IMINYL RADICALS, INHIBITORS, ACETYLOXIMES, DERIVATIVES, PYRIDINES, ACETONE, AGENTS",

author = "Fernando Portela-Cubillo and Scott, \{Jackie S.\} and Walton, \{John C.\}",

year = "2008",

doi = "10.1039/b803630f",

language = "English",

pages = "2935--2937",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "25",

}

TY - JOUR

T1 - 2-(aminoaryl)alkanone O-phenyl oximes: versatile reagents for syntheses of quinazolines

AU - Portela-Cubillo, Fernando

AU - Scott, Jackie S.

AU - Walton, John C.

PY - 2008

Y1 - 2008

N2 - Microwave irradiations of 2-(aminoaryl)alkanone O-phenyl oximes and carbonyl compounds generate iminyl radicals in company with imines; iminyl on imine ring closure yields dihydroquinazolines or quinazolines when ZnCl2 is included in the mixture.

AB - Microwave irradiations of 2-(aminoaryl)alkanone O-phenyl oximes and carbonyl compounds generate iminyl radicals in company with imines; iminyl on imine ring closure yields dihydroquinazolines or quinazolines when ZnCl2 is included in the mixture.

KW - RADICAL CYCLIZATION

KW - IMINYL RADICALS

KW - INHIBITORS

KW - ACETYLOXIMES

KW - DERIVATIVES

KW - PYRIDINES

KW - ACETONE

KW - AGENTS

UR - https://www.scopus.com/pages/publications/45549096875

U2 - 10.1039/b803630f

DO - 10.1039/b803630f

M3 - Article

SN - 1359-7345

SP - 2935

EP - 2937

JO - Chemical Communications

JF - Chemical Communications

IS - 25

ER -

2-(aminoaryl)alkanone O-phenyl oximes: versatile reagents for syntheses of quinazolines

Abstract

Keywords

Access to Document

Handle.net

Other files and links

Fingerprint

Cite this