Enhanced radical delivery from aldoxime esters for EPR and ring closure applications

AJ McCarroll; John Christopher Walton

Enhanced radical delivery from aldoxime esters for EPR and ring closure applications

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

Abstract

Arylmethaniminyl and alkyl radicals were generated from di- and tri-methoxyphenyl aldoxime esters, by photolysis in the presence of 4-methoxyacetophenone, and were detected by EPR spectroscopy: good yields of cyclised products were isolated from suitably unsaturated alkyl substituents.

Original language	English
Pages (from-to)	351-352
Number of pages	2
Journal	Chemical Communications
Publication status	Published - 2000

Keywords

IMINYL RADICALS

Cite this

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title = "Enhanced radical delivery from aldoxime esters for EPR and ring closure applications",

abstract = "Arylmethaniminyl and alkyl radicals were generated from di- and tri-methoxyphenyl aldoxime esters, by photolysis in the presence of 4-methoxyacetophenone, and were detected by EPR spectroscopy: good yields of cyclised products were isolated from suitably unsaturated alkyl substituents.",

keywords = "IMINYL RADICALS",

author = "AJ McCarroll and Walton, \{John Christopher\}",

year = "2000",

language = "English",

pages = "351--352",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

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T1 - Enhanced radical delivery from aldoxime esters for EPR and ring closure applications

AU - McCarroll, AJ

AU - Walton, John Christopher

PY - 2000

Y1 - 2000

N2 - Arylmethaniminyl and alkyl radicals were generated from di- and tri-methoxyphenyl aldoxime esters, by photolysis in the presence of 4-methoxyacetophenone, and were detected by EPR spectroscopy: good yields of cyclised products were isolated from suitably unsaturated alkyl substituents.

AB - Arylmethaniminyl and alkyl radicals were generated from di- and tri-methoxyphenyl aldoxime esters, by photolysis in the presence of 4-methoxyacetophenone, and were detected by EPR spectroscopy: good yields of cyclised products were isolated from suitably unsaturated alkyl substituents.

KW - IMINYL RADICALS

UR - https://www.scopus.com/pages/publications/0034615644

M3 - Article

SN - 1359-7345

SP - 351

EP - 352

JO - Chemical Communications

JF - Chemical Communications

ER -

Enhanced radical delivery from aldoxime esters for EPR and ring closure applications

Abstract

Keywords

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