Biochemical preparation of optically active 4-hydroxy-β-ionone and its transformation to (S)-6-hydroxy-α-ionone

Hideaki Kakeya, Takeshi Sugai, Hiromichi Ohta

研究成果: Article査読

21 被引用数 (Scopus)

抄録

The preparation of 4-hydroxy-β-ionone of high enantiomeric excess was achieved via lipase-catalyzed transesterification of the corresponding racemate as the key-step. Starting from Its (R)-enantiomer, (S)-6-hydroxy-α-ionone, an important intermediate for synthetic abscisic acid analogs, was synthesized.

本文言語English
ページ(範囲)1873-1876
ページ数4
ジャーナルAgricultural and biological chemistry
55
7
DOI
出版ステータスPublished - 1991 7月

ASJC Scopus subject areas

  • 生化学、遺伝学、分子生物学(全般)
  • 農業および生物科学(全般)

フィンガープリント

「Biochemical preparation of optically active 4-hydroxy-β-ionone and its transformation to (S)-6-hydroxy-α-ionone」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル