抄録
The first synthesis of the (9R,13R)-stereoisomer of LDS1, a flower-inducing oxylipin isolated from Lemna paucicostata, has been achieved from a known allylic alcohol by a seven-step sequence that involves the Horner-Wadsworth-Emmons olefination to construct its full carbon framework and an enzymatic hydrolysis of a penultimate methyl ester intermediate to provide the target molecule.
| 本文言語 | English |
|---|---|
| ページ（範囲） | 1459-1463 |
| ページ数 | 5 |
| ジャーナル | Bioscience, Biotechnology and Biochemistry |
| 巻 | 80 |
| 号 | 8 |
| DOI | |
| 出版ステータス | Published - 2016 |
ASJC Scopus subject areas
- バイオテクノロジー
- 分析化学
- 生化学
- 応用微生物学とバイオテクノロジー
- 分子生物学
- 有機化学