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Copper iodide Michael reactions

Promoted by copper iodide, a large array of 3-methylenetetrahydrofurans were synthesized from propargylic alkoxides as nucleophiles and activated alkenes as Michael acceptors. One of these reactions is shown below <02TL2609>. [Pg.189]

Addition (See also Michael reaction. Thiele reaction.) Acrolein. Cuprous chloride. Cuprous iodide. Diethylaluminum cyanide. Difluoramine. Dimethylcopper lithium. Methyl(tri-K-butylphosphine)copper complex. Methyl vinyl ketone. Rhodium trichloride. Sulfur dichloride. [Pg.511]

See other pages where Copper iodide Michael reactions is mentioned: [Pg.127]    [Pg.128]    [Pg.135]    [Pg.136]    [Pg.127]    [Pg.128]    [Pg.623]    [Pg.390]    [Pg.291]    [Pg.344]    [Pg.906]    [Pg.187]    [Pg.502]    [Pg.75]    [Pg.198]    [Pg.906]    [Pg.85]    [Pg.639]    [Pg.107]    [Pg.107]    [Pg.424]    [Pg.340]    [Pg.107]    [Pg.508]    [Pg.75]    [Pg.1297]    [Pg.508]    [Pg.345]   
See also in sourсe #XX -- [ Pg.189 ]



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