A short stereoselective synthesis of (-)-serricornin

Isao Shimizu, Kaoruko Hayashi, Masato Oshima

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Palladium-catalyzed reduction of (+)-(E)-(6S, 7S)-4,6-dimethyl-6,7-epoxy-4-nonen-3-one with formic acid gave (-)-(E)-(6S, 7S)-4,6-dimethyl-7-hydroxy-4-nonen-3-one, which was hydrogenated to give (-)-serricornin.

Original languageEnglish
Pages (from-to)4757-4758
Number of pages2
JournalTetrahedron Letters
Volume31
Issue number33
DOIs
Publication statusPublished - 1990

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formic acid
Palladium
serricornin

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

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A short stereoselective synthesis of (-)-serricornin. / Shimizu, Isao; Hayashi, Kaoruko; Oshima, Masato.

In: Tetrahedron Letters, Vol. 31, No. 33, 1990, p. 4757-4758.

Research output: Contribution to journalArticle

Shimizu, I, Hayashi, K & Oshima, M 1990, 'A short stereoselective synthesis of (-)-serricornin', Tetrahedron Letters, vol. 31, no. 33, pp. 4757-4758. https://doi.org/10.1016/S0040-4039(00)97725-6
Shimizu, Isao ; Hayashi, Kaoruko ; Oshima, Masato. / A short stereoselective synthesis of (-)-serricornin. In: Tetrahedron Letters. 1990 ; Vol. 31, No. 33. pp. 4757-4758.
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