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Chiral neomenthyl group

The first two observations indicate that the chiral phosphorus atom in VII dominates over the chiral neomenthyl group in determining the optical yield and absolute configuration of the hydrogenation product. [Pg.320]

An inviting chiral terminal group to use for this purpose is the neomenthyl group which is readily accessible from commercial (-)-menthol. Accordingly, we prepared the secondary phosphine (Nmen)-(C6H5)PH (VI) by the following sequence of reactions (Men = menthyl, Nmen = neomenthyl (28)) ... [Pg.317]

See other pages where Chiral neomenthyl group is mentioned: [Pg.317]    [Pg.318]    [Pg.258]    [Pg.378]    [Pg.317]    [Pg.318]    [Pg.258]    [Pg.378]    [Pg.120]    [Pg.310]    [Pg.319]    [Pg.13]    [Pg.153]    [Pg.1190]    [Pg.133]    [Pg.312]    [Pg.4924]    [Pg.618]    [Pg.4923]    [Pg.651]    [Pg.233]    [Pg.1204]    [Pg.54]   
See also in sourсe #XX -- [ Pg.153 ]



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Chiral group

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