## Abstract Several Manoalide analogs, 4‐(1‐acetyloxyalkyl)‐5‐hydroxy‐2(5H)‐furanones labeled with carbon‐14 in the alkyl side chain, were synthesized. The key step in these syntheses was singlet oxygenation of 2‐trialkylsilyl‐4‐alkylfurans to give the corresponding 4‐alkyl‐5‐hydroxy‐2(5H)‐furanone
✦ LIBER ✦
Synthesis of (S)-manoalide diol and the absolute configuration of natural manoalide
✍ Scribed by Victor Ekow Amoo; Silvano De Bernardo; Manfred Weigele
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 222 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
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