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

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10.1039/b803630f

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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",

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language = "English",

pages = "2935--2937",

journal = "Chemical Communications",

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publisher = "Royal Society of Chemistry",

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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

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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

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