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Propargyl alcohols carbomagnesiation

Duboudin s Cu-catalyzed anti carbomagnesiation of propargyl alcohol derivatives is one of still a small number of currently known carbometallation reactions of very high (>98%) regio- and stereoselectivity (Scheme 3.13b), which can be profitably exploited, as ejKmphfied by the efficient and highly selective synthesis of both (F)-and (Z)-y-bisabolenes (Scheme 3.35) [74]. [Pg.185]

Scheme 10 6 Synthesis of conjugated trienes by carbomagnesiation of enyne propargylic alcohols and ethers [71],... Scheme 10 6 Synthesis of conjugated trienes by carbomagnesiation of enyne propargylic alcohols and ethers [71],...
Scheme 10.89 Scope of the iron-catalyzed carbomagnesiation of (homo)propargylic alcohols [72]. Scheme 10.89 Scope of the iron-catalyzed carbomagnesiation of (homo)propargylic alcohols [72].
Considerably milder conditions for the regioselective carbomagnesiation of propargylic and homopropargylic alcohols were developed by Zhang and Ready... [Pg.822]


See other pages where Propargyl alcohols carbomagnesiation is mentioned: [Pg.646]    [Pg.648]    [Pg.648]    [Pg.652]    [Pg.652]    [Pg.878]    [Pg.19]    [Pg.15]    [Pg.822]    [Pg.823]   
See also in sourсe #XX -- [ Pg.645 , Pg.646 , Pg.647 , Pg.648 , Pg.649 , Pg.650 , Pg.651 ]




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