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Aromatic compounds asymmetric-transfer hydrogenation

A good number of reviews, perspectives, highlights, focus, and account of research were published in the period under review. The topics covered included nitfation of aromatic compounds, oxidation processes, Pd catalysis, oxidative coupling, asymmetric transfer hydrogenation, Sm-Barbier reaction, use of hypervalent I2, and Bayer-Villiger reaction. [Pg.91]

The asymmetric-transfer hydrogenation of aromatic compounds to enantiopure cyclic nitro compounds with two contiguous stereocentres in benzene is catalysed by H8-BfNOL-derived phosphoric acid with Hantzsch ester as the hydrogen source. The 1,4-// addition intermediate, formed in the initial step of the reaction, was isolated. The product is obtained with 97% yield and 99% ee. ... [Pg.157]

See other pages where Aromatic compounds asymmetric-transfer hydrogenation is mentioned: [Pg.80]    [Pg.44]    [Pg.98]    [Pg.32]    [Pg.80]    [Pg.411]    [Pg.216]    [Pg.32]    [Pg.26]    [Pg.964]    [Pg.964]    [Pg.151]    [Pg.92]    [Pg.393]    [Pg.280]    [Pg.184]    [Pg.248]    [Pg.277]   
See also in sourсe #XX -- [ Pg.157 ]



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Aromatic compounds hydrogenation

Aromatic compounds transfer hydrogenation

Aromatic hydrogen

Aromatic hydrogenation

Aromatics hydrogenation

Aromatization transfer-hydrogenation

Asymmetric hydrogenation aromatic

Asymmetric hydrogenation compounds

Asymmetric transfer

Asymmetric transfer hydrogenation

Asymmetric transfer hydrogenation aromatic

Compounds hydrogen

Hydrogen aromaticity

Hydrogenated aromatics

Hydrogenated compounds

Hydrogenation compounds

Hydrogenous compounds

Transfer hydrogenation aromatic

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