Stereo- and regio-selective formation of 2-oxazolone telomers as potential synthetic intermediates for aminosugars

Yoshihiro Abe, Takehisa Kunieda

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

3-Acetyl-2-oxazolone readily undergoes free-radical homopolymerization as well as telomerization with polyhalomethanes, in which low telomer formation is highly stereo- and regio-selective.

Original languageEnglish
Pages (from-to)5007-5010
Number of pages4
JournalTetrahedron Letters
Volume20
Issue number52
DOIs
Publication statusPublished - 1979
Externally publishedYes

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Oxazolone
Homopolymerization
Free Radicals

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Stereo- and regio-selective formation of 2-oxazolone telomers as potential synthetic intermediates for aminosugars. / Abe, Yoshihiro; Kunieda, Takehisa.

In: Tetrahedron Letters, Vol. 20, No. 52, 1979, p. 5007-5010.

Research output: Contribution to journalArticle

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