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Hydroamination of Simple, Nonactivated Alkenes

Hydroamination of Simple, Nonactivated Alkenes 349 Table 11.1 Lanthanocene catalyzed aminoalkene hydroamination/cyclization [35, 36]. [Pg.349]

As already mentioned, there has been significant progress in the development of chiral catalysts for asymmetric hydroamination reactions over the last decade. However, significant challenges remain, such as asymmetric intermolecular hydro aminations of simple nonactivated alkenes and the development of a chiral catalyst, which is applicable to a wide variety of substrates with consistent high stereochemical induction and tolerance of a multitude of functional groups as well as air and moisture. Certainly, late transition metal based catalysts show promising leads that could fill this void, but to date, early transition metal based catalysts (in particular, rare earth metals) remain the most active and most versatile catalyst systems. [Pg.369]


See other pages where Hydroamination of Simple, Nonactivated Alkenes is mentioned: [Pg.342]    [Pg.343]    [Pg.345]    [Pg.347]    [Pg.351]    [Pg.353]    [Pg.357]    [Pg.359]    [Pg.342]    [Pg.343]    [Pg.345]    [Pg.347]    [Pg.351]    [Pg.353]    [Pg.357]    [Pg.359]    [Pg.342]    [Pg.76]   


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Alkene simple

Alkenes hydroamination

Alkenes hydroaminations

Hydroamination

Hydroamination of Simple Alkenes

Hydroamination of alkenes

Hydroaminations

Nonactivated alkenes

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