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Bayer-Villiger lactone synthesis

Bamiphylline, 426 Bamipine, 51 Barbital, 267, 268 Barbiturates, listing, 268, 269 Baroreceptors, 54 Bayer-Villiger lactone synthesis, 28, 31... [Pg.477]

The first eiample of an Ireland-Qaisen rearrangement of an allyl lactone employed in natural product synthesis was that of Danishefsky and Tsuzuke in 1980 (Scheme 4.137) [132]. The allyl lactone possessed an exocyclic alkene, and hence resulted in a net 7-membered ring lactone to carbocycle conversion. A Bayer-Villiger reaction converted the pentenoic add to the 3° hydroxyl group of widdrol. [Pg.196]

See other pages where Bayer-Villiger lactone synthesis is mentioned: [Pg.108]    [Pg.452]    [Pg.1618]    [Pg.452]    [Pg.281]    [Pg.263]    [Pg.182]    [Pg.16]    [Pg.253]   
See also in sourсe #XX -- [ Pg.28 , Pg.31 ]



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