Transition-metal catalyzed oxidation of alcohols to aldehydes and ketones by means of Me3SiOOSiMe3

Shigekazu Kanemoto, Koichiro Oshima, Seijiro Matsubara, Kazuhiko Takai, Hitosi Nozaki

Research output: Contribution to journalArticle

74 Citations (Scopus)

Abstract

Pyridinium dichromate-Me3SiOOSiMe3 system has been found to be effective for the oxidation of alcohols to the corresponding carbonyl compounds. Selective oxidation of primary alcohols in the presence of secondary ones with RuCl2(PPh3)3-Me3SiOOSiMe3 is also described.

Original languageEnglish
Pages (from-to)2185-2188
Number of pages4
JournalTetrahedron Letters
Volume24
Issue number21
DOIs
Publication statusPublished - 1983
Externally publishedYes

Fingerprint

Ketones
Aldehydes
Transition metals
Metals
Alcohols
Carbonyl compounds
Oxidation
pyridinium dichromate

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Transition-metal catalyzed oxidation of alcohols to aldehydes and ketones by means of Me3SiOOSiMe3. / Kanemoto, Shigekazu; Oshima, Koichiro; Matsubara, Seijiro; Takai, Kazuhiko; Nozaki, Hitosi.

In: Tetrahedron Letters, Vol. 24, No. 21, 1983, p. 2185-2188.

Research output: Contribution to journalArticle

Kanemoto, Shigekazu ; Oshima, Koichiro ; Matsubara, Seijiro ; Takai, Kazuhiko ; Nozaki, Hitosi. / Transition-metal catalyzed oxidation of alcohols to aldehydes and ketones by means of Me3SiOOSiMe3. In: Tetrahedron Letters. 1983 ; Vol. 24, No. 21. pp. 2185-2188.
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