Nucleophilic substitution reaction at the nitrogen of arylsulfonamides with phosphide anion

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

A novel nucleophilic substitution reaction at the nitrogen of arylsulfonamides by means of phosphide anions has been described. This reaction allows for the efficient transformation of arylsulfonamides into synthetically valuable phosphamides, amines, and a variety of protected amines.

Original languageEnglish
Pages (from-to)19358-19361
Number of pages4
JournalJournal of the American Chemical Society
Volume134
Issue number47
DOIs
Publication statusPublished - Nov 28 2012

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Amines
Anions
Substitution reactions
Nitrogen
Negative ions
Dimethoate

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)
  • Biochemistry
  • Colloid and Surface Chemistry

Cite this

Nucleophilic substitution reaction at the nitrogen of arylsulfonamides with phosphide anion. / Yoshida, Suguru; Igawa, Kazunobu; Tomooka, Katsuhiko.

In: Journal of the American Chemical Society, Vol. 134, No. 47, 28.11.2012, p. 19358-19361.

Research output: Contribution to journalArticle

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