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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

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✦ 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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