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Chromium, allylic 1,2-asymmetric induction

Allylic Chromium Reagents 12-Asymmetric Induction fAnti/Syn Control)... [Pg.173]

Maguire, R. J., Mulzer, J., Bats, J. W. 1,4-Asymmetric Induction in the Chromium(ll)-and Indium-Mediated Coupling of Allyl Bromides to Aldehydes. J. Org. Chem. 1996, 61, 6936-6940. [Pg.642]

Asymmetric induction at an allylic centre in the side-chain of a phenolic ether in the form of its chromium tricarbonyl complex has been described. The chiral... [Pg.101]

In the 15 years since Fiirstner et al. developed the first NHK reaction using catalytic quantities of chromium, the subsequent stereoselective, catalytic variant has become a valuable tool in catalytic asymmetric synthesis. Many studies on the NHK reaction have focused on the application of ligands that have proven successful in a range of other catalytic asymmetric processes. For example, the salen- and oxazoline-derived ligands that have been applied have advanced the scope of the NHK reaction in terms of reactivity and asymmetric induction in a wide array of carbon-carbon forming processes. These processes now include allylation, crotylation, vinylation, methallylation, aUenylation, homoallenylation, and propargylation. Xia and Yamamoto s TBOxCr(III)Cl complex has afforded some of the highest levels of enantioselectivity in a series of allylation, crotylation, aUenylation, and more recent dienylation and alkynylation studies. [Pg.365]


See other pages where Chromium, allylic 1,2-asymmetric induction is mentioned: [Pg.224]    [Pg.189]    [Pg.189]    [Pg.371]    [Pg.189]    [Pg.155]    [Pg.244]   
See also in sourсe #XX -- [ Pg.187 ]

See also in sourсe #XX -- [ Pg.187 ]

See also in sourсe #XX -- [ Pg.187 ]

See also in sourсe #XX -- [ Pg.187 ]

See also in sourсe #XX -- [ Pg.187 ]




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