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Catalytic performances production from alcohols

Catalytic Performances of Perovskite-Type Catalysts for H2 Production from Alcohols 1549... [Pg.549]

ADHs were screened for this purpose and ADH-A from Rhodoccocus ruber could furnish the (S)-enantiomer with perfect enantiopurity (>99% ee) and 93% isolated yield. Reducing equivalents were provided by isopropanol in a coupled-substrate approach and allowed the use of catalytic amounts of NADH. The product from the enzymatic reduction required stereoinversion of the stereogenic center en route to the more active (R)-form of ramatroban. This was performed by converting the alcohol into the amine via the azide form, in a combined Mitsunobu-Staudinger one-pot reaction at low temperature [27]. [Pg.341]

See other pages where Catalytic performances production from alcohols is mentioned: [Pg.417]    [Pg.32]    [Pg.33]    [Pg.77]    [Pg.119]    [Pg.119]    [Pg.126]    [Pg.645]    [Pg.82]    [Pg.330]    [Pg.360]    [Pg.330]    [Pg.360]    [Pg.119]    [Pg.309]    [Pg.135]    [Pg.1257]    [Pg.164]    [Pg.297]    [Pg.280]    [Pg.6]    [Pg.151]    [Pg.127]    [Pg.420]    [Pg.649]    [Pg.664]    [Pg.12]    [Pg.56]    [Pg.330]    [Pg.501]    [Pg.257]    [Pg.58]    [Pg.727]    [Pg.178]    [Pg.300]    [Pg.119]    [Pg.229]    [Pg.500]    [Pg.166]    [Pg.395]    [Pg.54]    [Pg.53]    [Pg.67]    [Pg.395]    [Pg.1]    [Pg.126]    [Pg.344]   


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Alcohols production

Catalytic Performances of Perovskite-Type Catalysts for H2 Production from Alcohols

Catalytic products from

Product performance

Production performance

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