Synthesis and reactivity of stable trisyl(aminomethylphenyl)silylenoid

Hyeon Mo Cho, Young Mook Lim, Byung Wook Lee, Sung Jin Park, Myong Euy Lee

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

A highly thermally stable silylenoid, trisyl(aminomethylphenyl)silylenoid (2) was synthesized from the reaction of dimethylaminomethylphenyllithium with a bromosilylenoid, 1. Silylenoid 2 reacted with electrophiles to give the corresponding products, but did not react with alkyllithiums as a nucleophile.

Original languageEnglish
Pages (from-to)2665-2668
Number of pages4
JournalJournal of Organometallic Chemistry
Volume696
Issue number13
DOIs
Publication statusPublished - 2011 Jul 1

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Nucleophiles
nucleophiles
reactivity
synthesis
products

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry
  • Materials Chemistry

Cite this

Cho, Hyeon Mo ; Lim, Young Mook ; Lee, Byung Wook ; Park, Sung Jin ; Lee, Myong Euy. / Synthesis and reactivity of stable trisyl(aminomethylphenyl)silylenoid. In: Journal of Organometallic Chemistry. 2011 ; Vol. 696, No. 13. pp. 2665-2668.
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Synthesis and reactivity of stable trisyl(aminomethylphenyl)silylenoid. / Cho, Hyeon Mo; Lim, Young Mook; Lee, Byung Wook; Park, Sung Jin; Lee, Myong Euy.

In: Journal of Organometallic Chemistry, Vol. 696, No. 13, 01.07.2011, p. 2665-2668.

Research output: Contribution to journalArticle

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AU - Lee, Myong Euy

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