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Reformatsky reaction thermodynamic stereoselection

Because of conflicting reports or inadequate controls, the question of kinetic or thermodynamic control of stereochemistry for reported Reformatsky reactions often has no satisfactory answer. Jacques and co-workers have concluded that Reformatsky reactions of benzaldehyde in refluxing benzene can be completed with kinetic stereoselection. The relatively high syn.anti ratios they observed, at least with small R groups (equation 36 and Table 4), are not those expected for equilibrated zinc chelates. [Pg.291]


See other pages where Reformatsky reaction thermodynamic stereoselection is mentioned: [Pg.217]    [Pg.217]    [Pg.6362]    [Pg.77]    [Pg.449]   
See also in sourсe #XX -- [ Pg.2 , Pg.289 ]

See also in sourсe #XX -- [ Pg.289 ]

See also in sourсe #XX -- [ Pg.289 ]

See also in sourсe #XX -- [ Pg.2 , Pg.289 ]

See also in sourсe #XX -- [ Pg.289 ]




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