Amidoethylation of Anthracene Hydride by N-Aroylaziridines: Inner-sphere Single Electron Transfer (SET) and Radical Coupling confirmed

P. Y. Lin, H. Stamm

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Regioselectivity (near 1:1) of substitutive ring opening of 1-benzoyl-2-methylaziridine by anthracene hydride is incompatible with common nucleophilic attack and thus confirms the radical coupling path.

Original languageEnglish
Pages (from-to)646-647
Number of pages2
JournalJournal of Chemical Research - Part S
Issue number10
Publication statusPublished - 1998
Externally publishedYes

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Regioselectivity
Hydrides
Electrons
anthracene
propyleneimine

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

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title = "Amidoethylation of Anthracene Hydride by N-Aroylaziridines: Inner-sphere Single Electron Transfer (SET) and Radical Coupling confirmed",
abstract = "Regioselectivity (near 1:1) of substitutive ring opening of 1-benzoyl-2-methylaziridine by anthracene hydride is incompatible with common nucleophilic attack and thus confirms the radical coupling path.",
author = "Lin, {P. Y.} and H. Stamm",
year = "1998",
language = "English",
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journal = "Journal of Chemical Research - Part S",
issn = "0308-2342",
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T2 - Inner-sphere Single Electron Transfer (SET) and Radical Coupling confirmed

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AU - Stamm, H.

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Y1 - 1998

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AB - Regioselectivity (near 1:1) of substitutive ring opening of 1-benzoyl-2-methylaziridine by anthracene hydride is incompatible with common nucleophilic attack and thus confirms the radical coupling path.

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JO - Journal of Chemical Research - Part S

JF - Journal of Chemical Research - Part S

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