Ethers, famesyl synthesis

An intramolecular cycloaddition of the tetradecatrienyl nitroethyl ether 263 was used in the synthesis of the 14-membered bicyclic precursor 265 of crassin acetate 266, a cembrane lactone possessing antibiotic and antineoplastic activity (332). Nitro compound 263 was obtained from famesyl acetate (262) in several steps and was then treated with phenyl isocyanate and triethylamine to give the tricyclic isoxazoline 264 (Scheme 6.98). Conversion to ketone 265 was accomplished by hydrogenation of the cycloadduct with Raney Ni and boric acid followed by acetylation (332). In this case, the isoxazoline derived from a 3-butenyl nitroethyl ether moiety served to produce a 3-methylenetetrahydropyran moiety (332). 

Marriott JH, Moreno Barber AM, Hardcastle IR, Rowlands MG, Grimshaw RM, Neidle S, Jarman M. Synthesis of the famesyl ether 2,3,5-trilluoro-6-hydroxy-4-((E,E.-3,7,ll-trimethyldodeca-2,... 

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