SYnthesis and absolute configuration of (−)-pentalenolactone E methyl ester
✍ Scribed by Kenji Mori; Masahiro Tsuji
- Book ID
- 104207279
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 737 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
✦ Synopsis
The naturally occurruq enantlomer of peatalenolactone E was synthesized as Its levorotatory Me ester 1 starting from (+)-2-ethoxycarbonyl-7,7-ethylenedioxyblcyclo[3.3.0loctan-3-one 3, which was obtarrxl by treatng (?)-3 with baker's yeast. The absolute configuration of pentalenolactone E Me ester was established as depicted In 1.
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