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Allyl partial rate factors

Kinetic resolution.l33 Since enantiomers react with chiral compounds at different rates, it is sometimes possible to effect a partial separation by stopping the reaction before completion. This method is very similar to the asymmetric syntheses discussed on p. 102. An important application of this method is the resolution of racemic alkenes by treatment with optically active diisopinocampheylborane,134 since alkenes do not easily lend themselves to conversion to diastereomers if no other functional groups are present. Another example is the resolution of allylic alcohols such as 45 with one enantiomer of a chiral epoxidizing agent (see 5-36).135 In the case of 45 the discrimination was extreme. One enantiomer was converted to the epoxide and the other was not, the rate ratio (hence the selectivity factor)... [Pg.124]


See other pages where Allyl partial rate factors is mentioned: [Pg.197]    [Pg.425]    [Pg.168]    [Pg.499]    [Pg.627]    [Pg.343]    [Pg.826]    [Pg.42]    [Pg.631]    [Pg.627]    [Pg.174]    [Pg.502]    [Pg.551]   
See also in sourсe #XX -- [ Pg.156 ]




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Partial rate factors

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