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Camphor, molecular model

Camphor, molecular model of, 129 specific rotation of, 296 Cannizzaro, Stanislao, 724 Cannizzaro reaction. 724 mechanism of, 724 Caprolactam, nylon 6 from, 1213 Capsaicin, structure of. 78 -curbahlehyde, aldehyde name ending, 696... [Pg.1289]

Asymmetric hydrosilylation can be accomplished (i) by [RhO(PPh3)3] if the organic substrate is optically active, e.g. (-)-menthane or ( + )-camphor, or (ii) if chiral phosphine-rhodium catalysts are used. In the particular case where the catalyst is a (diop)rhodium(i) derivative molecular models of intermediates based on oxidative addition of the silane to Rh, e.g. (61), can be used to predict the chirality of products... [Pg.373]

See other pages where Camphor, molecular model is mentioned: [Pg.130]    [Pg.130]    [Pg.482]    [Pg.134]    [Pg.339]    [Pg.363]    [Pg.172]    [Pg.363]    [Pg.407]    [Pg.519]    [Pg.40]    [Pg.212]    [Pg.1368]    [Pg.50]    [Pg.9]    [Pg.362]    [Pg.453]   
See also in sourсe #XX -- [ Pg.129 ]

See also in sourсe #XX -- [ Pg.129 ]

See also in sourсe #XX -- [ Pg.131 ]



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Camphorates

Camphore

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