- A CONCISE SYNTHESIS OF (R)-HYDROXY-E,Z-DIENE FATTY ACIDS: PREPARATION OF 12(R)-HETE, TETRANOR-12(R)-HETE, AND 13(R)-HODE
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Chiral E-enals derived from functionalized 2-deoxy-D-ribofuranoses by ylide-induced β-elimination were exploited for the synthesis of fatty acid metabolites containing (R)-hydroxy-E,Z-diene subunit.
- Lumin, Sun,Falck, J. R.,Schwartzman, Michal L.
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p. 2315 - 2318
(2007/10/02)
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- Prostaglandin Analogues Possessing Antinidatory Effects. 2. Modification of the α Chain
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Additional double bonds were introduced into the α chain in 16-phenoxy-, 16-(3-chlorophenoxy)-, 16--, and 16-(4-chlorophenoxy)-17,18,19,20-tetranorprostaglandins which have antinidatory effects.Of these analogues, the Δ3/
- Hayashi, Masaki,Arai, Yoshinobu,Wakatsuka, Hirohisa,Kawamura, Masanori,Konishi, Yoshitaka,et al.
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p. 525 - 535
(2007/10/02)
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