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Diels-Alder reactions butadiene-2-carboxylic ester

Several cycloaddition reactions of 2,5-dihydrothiophene derivatives have been reported. Compounds possessing an enamine system undergo [2 + 2] cycloaddition with acetylene-dicarboxylic ester (Scheme 215) (77AHC(2l)253). Diels-Alder addition of the 2,5-di-hydrothiophene-3-carboxylic ester (557) with butadiene, followed by desulfurization, leads to the trisubstituted cyclohexane (558) (B-74MI31404). [Pg.850]


See other pages where Diels-Alder reactions butadiene-2-carboxylic ester is mentioned: [Pg.351]    [Pg.355]    [Pg.351]    [Pg.390]    [Pg.393]    [Pg.337]    [Pg.355]    [Pg.473]    [Pg.475]    [Pg.552]   
See also in sourсe #XX -- [ Pg.301 ]




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