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Aryl derivatives solid support catalysts

Comparable levels of selectivity (s = 7.6-24) can also be achieved for the KR of a similar range of aryl alkyl sec-alcohols using Yamada s reasonably readily accessed chiral thiazolidine-2-thione-based DMAP 19 (Fig. 8.4) at between 0 °C and rt over 3 to 12 h [100]. The N-(4/-pyridinyl)-a-methylproline derived catalysts 16, and the solid-supported variant 17 (Fig. 8.4) developed by Campbell [95-98]... [Pg.294]


See other pages where Aryl derivatives solid support catalysts is mentioned: [Pg.962]    [Pg.343]    [Pg.151]    [Pg.298]    [Pg.20]    [Pg.625]    [Pg.49]    [Pg.551]    [Pg.199]    [Pg.363]    [Pg.673]    [Pg.120]   


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Aryl derivatives

Aryl derivs

Arylation derivatives

Catalyst solid supported

Catalysts solid

Solid support

Solid support catalysts

Solid-supported

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