Alkylation of 2-phenylsulfinylethanol

Ohta Hiromichi, Matsumoto Shinsuke, Takeshi Sugai

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Alkylation of 2-phenylsulfinylethanol resulted syndiastereomer as the major products, although the ratio of syn/anti isomers varied depending on the alkyl groups. By application of this procedure to the chiral sulfoxides, optically active epoxides have been obtained in good yields.

Original languageEnglish
Pages (from-to)2895-2898
Number of pages4
JournalTetrahedron Letters
Volume31
Issue number20
DOIs
Publication statusPublished - 1990

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Sulfoxides
Epoxy Compounds
Alkylation
Isomers

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Alkylation of 2-phenylsulfinylethanol. / Hiromichi, Ohta; Shinsuke, Matsumoto; Sugai, Takeshi.

In: Tetrahedron Letters, Vol. 31, No. 20, 1990, p. 2895-2898.

Research output: Contribution to journalArticle

Hiromichi, Ohta ; Shinsuke, Matsumoto ; Sugai, Takeshi. / Alkylation of 2-phenylsulfinylethanol. In: Tetrahedron Letters. 1990 ; Vol. 31, No. 20. pp. 2895-2898.
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