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Rhodium carbene reactions natural products

Carbonyl ylides can be viewed as an adduct between a carbonyl group and a carbene and, in fact, some ylides have been prepared this way (see above). The application of carbonyl ylides to the synthesis of complex natural products has been greatly advanced by the finding that stabilized carbenoids can be generated by the decomposition of ot-diazocarbonyl compounds with copper and rhodium complexes. The metallocarbenoids formed by this method are highly electrophilic on carbon and readily add nucleophiles such as the oxygen of many carbonyl derivatives to form carbonyl ylides. This type of reaction is in fact quite old with the first report being the addition of diazomalonate and benzaldehyde (33,34). [Pg.269]


See other pages where Rhodium carbene reactions natural products is mentioned: [Pg.242]    [Pg.369]    [Pg.157]    [Pg.151]    [Pg.76]    [Pg.309]    [Pg.257]    [Pg.864]    [Pg.866]    [Pg.130]    [Pg.784]    [Pg.784]    [Pg.87]   
See also in sourсe #XX -- [ Pg.32 , Pg.33 , Pg.34 , Pg.111 , Pg.273 , Pg.324 , Pg.326 , Pg.327 , Pg.328 , Pg.329 , Pg.348 ]




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