Synthesis of (5)-2-hydroxy-/?-ionone, employing (5)-3-hydroxy-2,2-dimethylcyclohexanone as the chiral starting material

Makoto Yanai, Takeshi Sugai, Kenji Mori

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

(S)-2-Hydroxy-/?-ionone of 96% e.e. was synthesized from (S)-3-hydroxy-2,2-dimethyl- cyclohexanone, which was easily obtained by the baker’s yeast reduction of 2,2-dimethylcyclo- hexane-l,3-dione.

Original languageEnglish
Pages (from-to)2373-2377
Number of pages5
JournalAgricultural and Biological Chemistry
Volume49
Issue number8
DOIs
Publication statusPublished - 1985
Externally publishedYes

Fingerprint

Norisoprenoids
norisoprenoids
bakers yeast
Hexanes
Yeast
hexane
Saccharomyces cerevisiae
synthesis
cyclohexanones
cyclohexanone

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

Synthesis of (5)-2-hydroxy-/?-ionone, employing (5)-3-hydroxy-2,2-dimethylcyclohexanone as the chiral starting material. / Yanai, Makoto; Sugai, Takeshi; Mori, Kenji.

In: Agricultural and Biological Chemistry, Vol. 49, No. 8, 1985, p. 2373-2377.

Research output: Contribution to journalArticle

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