A mild and environmentally benign oxidation of thiols to disulfides

Masayuki Kirihara, Yasutaka Asai, Shiho Ogawa, Takuya Noguchi, Akihiko Hatano, Yoshiro Hirai

Research output: Contribution to journalArticle

140 Citations (Scopus)

Abstract

Thiols were effectively oxidized into disulfides by reacting with hydrogen peroxide in the presence of a catalytic amount of iodide ion or iodine.

Original languageEnglish
Article numberF15107SS
Pages (from-to)3286-3289
Number of pages4
JournalSynthesis
Issue number21
DOIs
Publication statusPublished - 2007 Nov 2
Externally publishedYes

Fingerprint

Iodides
Iodine
Sulfhydryl Compounds
Hydrogen peroxide
Disulfides
Hydrogen Peroxide
Ions
Oxidation

Keywords

  • Disulfide
  • Hydrogen peroxide
  • Iodide catalyst
  • Oxidative coupling
  • Thiol

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Kirihara, M., Asai, Y., Ogawa, S., Noguchi, T., Hatano, A., & Hirai, Y. (2007). A mild and environmentally benign oxidation of thiols to disulfides. Synthesis, (21), 3286-3289. [F15107SS]. https://doi.org/10.1055/s-2007-990800

A mild and environmentally benign oxidation of thiols to disulfides. / Kirihara, Masayuki; Asai, Yasutaka; Ogawa, Shiho; Noguchi, Takuya; Hatano, Akihiko; Hirai, Yoshiro.

In: Synthesis, No. 21, F15107SS, 02.11.2007, p. 3286-3289.

Research output: Contribution to journalArticle

Kirihara, M, Asai, Y, Ogawa, S, Noguchi, T, Hatano, A & Hirai, Y 2007, 'A mild and environmentally benign oxidation of thiols to disulfides', Synthesis, no. 21, F15107SS, pp. 3286-3289. https://doi.org/10.1055/s-2007-990800
Kirihara M, Asai Y, Ogawa S, Noguchi T, Hatano A, Hirai Y. A mild and environmentally benign oxidation of thiols to disulfides. Synthesis. 2007 Nov 2;(21):3286-3289. F15107SS. https://doi.org/10.1055/s-2007-990800
Kirihara, Masayuki ; Asai, Yasutaka ; Ogawa, Shiho ; Noguchi, Takuya ; Hatano, Akihiko ; Hirai, Yoshiro. / A mild and environmentally benign oxidation of thiols to disulfides. In: Synthesis. 2007 ; No. 21. pp. 3286-3289.
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