Radical combination in the ortho position of trityl radical observed in single-electron transfer reactions of trityl anion

Jürgen Werry, Pen Yuan Lin, Konstantinos Bellos, Petros Assithianakis, Helmut Stamm

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Single-electron transfer reactions between trityl anion and 1-acyl-2,2-dimethylaziridines provide, among other products, the methallyl amides 7 and the triphenylmethanes 8 carrying an amidoethyl chain attached with the tertiary carbon ortho to the triphenylmethane.

Original languageEnglish
Pages (from-to)1389-1390
Number of pages2
JournalJournal of the Chemical Society, Chemical Communications
Issue number20
DOIs
Publication statusPublished - 1990
Externally publishedYes

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Amides
Anions
Negative ions
Electrons
Carbon
triphenylmethane

ASJC Scopus subject areas

  • Molecular Medicine

Cite this

Radical combination in the ortho position of trityl radical observed in single-electron transfer reactions of trityl anion. / Werry, Jürgen; Lin, Pen Yuan; Bellos, Konstantinos; Assithianakis, Petros; Stamm, Helmut.

In: Journal of the Chemical Society, Chemical Communications, No. 20, 1990, p. 1389-1390.

Research output: Contribution to journalArticle

Werry, Jürgen ; Lin, Pen Yuan ; Bellos, Konstantinos ; Assithianakis, Petros ; Stamm, Helmut. / Radical combination in the ortho position of trityl radical observed in single-electron transfer reactions of trityl anion. In: Journal of the Chemical Society, Chemical Communications. 1990 ; No. 20. pp. 1389-1390.
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