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- W2951279454 abstract "The naturally occurring macrolide, (±)-recifeiolide, was synthesized stereoselectively. (E)-11-Hydroxy-8-dodecenoic acid (5) was obtained stereoselectively from 11-hydroxy-8-dodecynoic acid by the reduction with lithium, and the acid (5) was cyclized to (±)-recifeiolide in excellent yield via its 6-phenyl-2-pyridyl ester. Similarly, (R)-(+)-ricinelaidic acid was lactonized to afford the corresponding lactone in high yield." @default.
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- W2951279454 date "1978-03-28" @default.
- W2951279454 modified "2023-09-26" @default.
- W2951279454 title "ChemInform Abstract: STEREOSELECTIVE TOTAL SYNTHESES OF (.+-.)-RECIFEIOLIDE AND (R)-(+)-RICINELAIDIC ACID LACTONE" @default.
- W2951279454 cites W2059908883 @default.
- W2951279454 doi "https://doi.org/10.1002/chin.197813237" @default.
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