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Enantiomers transition state analogues

A similar approach was employed in our laboratory for the development of molecularly imprinted catalysts for the enantio-selective reduction of prochiral ketones with borane (CBS reaction) [122]. A stable, polymerisable transition state analogue of this reaction leading to the formation of one particular enantiomer product was prepared (Fig. 4.9). After polymerisation, the template molecule can... [Pg.106]

See other pages where Enantiomers transition state analogues is mentioned: [Pg.198]    [Pg.58]    [Pg.258]    [Pg.294]    [Pg.127]    [Pg.43]    [Pg.103]    [Pg.216]    [Pg.104]    [Pg.262]    [Pg.103]    [Pg.122]    [Pg.342]    [Pg.161]    [Pg.546]    [Pg.546]    [Pg.312]    [Pg.628]    [Pg.7]    [Pg.405]    [Pg.175]    [Pg.411]    [Pg.476]    [Pg.411]    [Pg.476]   
See also in sourсe #XX -- [ Pg.127 ]



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Transition analogues

Transition state analogues

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