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Elimination reactions conjugated epoxides

Dienes from epoxides. In refluxing dichloroethane in the presence of triethyl-amine, epoxides undergo a double-elimination reaction, giving conjugated dienes in good yields. Crowded epoxides remain unchanged thus, the mixture of cis- and frani-cyclododecene oxides affords a clean mixture of (IE, 3Z)-cyclododecadiene and rran -cyclododecene oxide (50% yield). [Pg.42]


See other pages where Elimination reactions conjugated epoxides is mentioned: [Pg.391]    [Pg.391]    [Pg.744]    [Pg.220]    [Pg.428]    [Pg.113]    [Pg.129]    [Pg.700]    [Pg.138]    [Pg.376]    [Pg.195]    [Pg.210]    [Pg.1477]    [Pg.550]    [Pg.407]    [Pg.173]    [Pg.344]    [Pg.173]    [Pg.187]    [Pg.354]    [Pg.1518]    [Pg.550]    [Pg.2065]    [Pg.776]    [Pg.776]    [Pg.72]    [Pg.167]    [Pg.186]    [Pg.98]    [Pg.123]    [Pg.62]    [Pg.123]    [Pg.424]    [Pg.530]    [Pg.776]    [Pg.100]    [Pg.1091]    [Pg.49]    [Pg.105]    [Pg.272]    [Pg.19]    [Pg.333]    [Pg.171]    [Pg.76]    [Pg.399]   
See also in sourсe #XX -- [ Pg.231 ]




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Conjugate reaction

Conjugated reaction

Conjugative reactions

Elimination conjugate

Elimination reactions conjugative

Epoxide reaction

Epoxides reactions

Reactions epoxidation

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