The synthesis of 2,3-dinor-6-oxo-prostaglandin F,c, the major metabolite of prostacyclin, from the prostaglandin lactone intermediate ( 2) is reported.
Short synthesis of 6-oxoprostaglandin E1 and 6-oxoprostaglandin F1α
✍ Scribed by T. Tanaka; A. Hazato; K. Bannai; N. Okamura; S. Sugiura; K. Manabe; S. Kurozumi; M. Suzuki; R. Noyori
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- French
- Weight
- 273 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
El methyl ester was synthesized in a single pot from (R)-4-cbutyldimethylsiloxy-2-cyclopentenone by organocopper conjugate addition with an w side-chain unit, trapping of the resulting enolate with 6-methoxycarbonyl-2-nitrohex-1-ene, and treatment with aqueous titanium (III) trichloride. Hydrolysis of the methyl ester was accomplished by porcine liver esterase.
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