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Mukaiyama aldol reaction synthetic utility

The synthetic utility of the Mukaiyama aldol reaction is broadened when coupled with other reactions in a tandem fashion. Romo and coworkers developed a highly diastereoselective tandem Mukaiyama aldol-lactonization... [Pg.512]

An important reaction of silylenol ethers is their use as enolate equivalent in Mukaiyama aldol additions. An example of the synthetic utility of this reaction with a magnesium enolate as starting reagent is shown below. [Pg.473]

See other pages where Mukaiyama aldol reaction synthetic utility is mentioned: [Pg.102]    [Pg.102]    [Pg.107]    [Pg.298]    [Pg.409]    [Pg.103]    [Pg.84]    [Pg.103]    [Pg.502]   
See also in sourсe #XX -- [ Pg.504 , Pg.505 , Pg.506 , Pg.507 , Pg.508 , Pg.509 , Pg.510 , Pg.511 , Pg.512 , Pg.513 , Pg.514 , Pg.515 , Pg.516 ]



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