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2-alkoxy-3- - 2-alkoxyalkanoate ester

A wide range of organic substrates can undergo an oxidative carbonylation reaction. Depending on reaction conditions, alkenes have been converted into -chloroalkanoyl chlorides (oxidative chloro-chlorocarbonylation) [1,2], succinic diesters (oxidative dialkoxycarbonylation) [3-20], a,/J-unsaturated esters [21,22] (oxidative monoalkoxycarbonylation), or /J-alkoxyalkanoic esters [11] (oxidative alkoxy-alkoxycarbonylation), according to Eqs. 10-13. [Pg.246]


See other pages where 2-alkoxy-3- - 2-alkoxyalkanoate ester is mentioned: [Pg.2006]    [Pg.2060]    [Pg.2149]    [Pg.2149]    [Pg.2149]    [Pg.2149]    [Pg.2149]    [Pg.2150]    [Pg.2150]    [Pg.2156]    [Pg.2156]    [Pg.2180]    [Pg.2180]    [Pg.2006]    [Pg.2149]    [Pg.2149]    [Pg.2149]    [Pg.2149]    [Pg.2149]    [Pg.2150]    [Pg.2150]    [Pg.2150]    [Pg.2150]    [Pg.2150]    [Pg.2156]    [Pg.2156]    [Pg.2174]    [Pg.2180]    [Pg.2180]    [Pg.1097]    [Pg.1109]    [Pg.2396]    [Pg.2396]    [Pg.2396]   
See also in sourсe #XX -- [ Pg.1733 ]




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Alkoxy ester

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