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Chiral 1,2-Disubstituted Ferrocenyl Aminoalcohols

The chiral vinylferrocene monomer 18 and the chiral copolymers 19a — e have been prepared for the first time. Insolubilization of the chiral ferrocene catalyst lowered the enantioselectivity to some extent compared with that of the soluble monomeric catalysts. Nevertheless, polymers 19a —e are usefull for the enantiose-lective synthesis of secondary alcohols. [Pg.153]


See other pages where Chiral 1,2-Disubstituted Ferrocenyl Aminoalcohols is mentioned: [Pg.153]    [Pg.153]    [Pg.155]    [Pg.157]    [Pg.161]    [Pg.163]    [Pg.165]    [Pg.153]    [Pg.155]    [Pg.157]    [Pg.161]    [Pg.163]    [Pg.165]    [Pg.153]    [Pg.153]    [Pg.155]    [Pg.157]    [Pg.161]    [Pg.163]    [Pg.165]    [Pg.153]    [Pg.155]    [Pg.157]    [Pg.161]    [Pg.163]    [Pg.165]    [Pg.420]   


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1,2-disubstituted ferrocenyl aminoalcohol

2,2-disubstituted, chiral

Aminoalcohol

Chiral aminoalcohols

Chiral ferrocenyl aminoalcohols

Ferrocenyl

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