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Trimethylsilyl-ynones

Utimoto et al. [145] reported a procedure for the synthesis of macrocyclic ynones by intramolecular acylation of )-(trimethylsilyl)ethynylalkanoyl chlorides in the presence of Lewis acid. For example, in the synthesis of f — )-muscone 216), cyclization of alkyne acid chloride 238 gave the macrocycle 239 in 52% yield, which was hydrogenated to f — )-muscone (Scheme 80). [Pg.158]


See other pages where Trimethylsilyl-ynones is mentioned: [Pg.563]    [Pg.34]    [Pg.876]    [Pg.221]    [Pg.221]    [Pg.1088]    [Pg.49]    [Pg.63]    [Pg.34]    [Pg.448]    [Pg.154]    [Pg.139]    [Pg.396]    [Pg.326]   
See also in sourсe #XX -- [ Pg.396 ]




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