Sharpless chiral epoxidation of the ethyl esters of (2E,4E,6Z) -, (2E,4E,6E)-and (2E,4Z,GE)-8-hydroxy-9-methyldeca-2,4,6,9-tetraenoic acid gave predominantly the (8R,9S)epoxyalcohols. These were converted into the host-specific plant toxins AF Ila, AF Ilc and AK II, thereby effecting a total synthes
Chiral synthesis of a key intermediate in the preparation of the AF toxin IIc
✍ Scribed by Mohammed Laabassi; René Grée
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 247 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
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