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Chiral poisoning, asymmetric amplification

Related concepts asymmetric amplification chiral poisoning asymmetric activation... [Pg.152]

VII. Asymmetric amplification in chiral poisoning or chiral activation of a racemic catalyst... [Pg.257]

VII. ASYMMETRIC AMPLIFICATION IN CHIRAL POISONING OR CHIRAL ACTIVATION OF A RACEMIC CATALYST... [Pg.287]

Faller, J. W., Sams, D. W. I., Liu, X. Catalytic Asymmetric Synthesis of Homoallylic Alcohols Chiral Amplification and Chiral Poisoning in a Titanium/BINOL Catalyst System. J. Am. Chem. Soc. 1996,118, 1217-1218. [Pg.612]

The reaction of methallyltri-n-butylstannane 117 with achiral aldehydes is also effectively promoted by the binol-Ti complex [89 c]. In all but one case (cyclo-hexanecarboxaldehyde), the yields and enantioselectivities observed with the methallylstannane are identical or higher than those obtained in the reactions with allyltributylstannane with only 10 mol% of the binol-Ti complex (Scheme 10-50). Insight into the nature of the titanium catalyst is provided by the observation of asymmetric amplification [89 b] and chiral poisoning [89 g]. An intruiging hypothesis on the origin of enantioselection in allylation and related reactions [89 h]. [Pg.339]


See other pages where Chiral poisoning, asymmetric amplification is mentioned: [Pg.152]    [Pg.222]    [Pg.478]    [Pg.220]    [Pg.250]   
See also in sourсe #XX -- [ Pg.287 , Pg.288 ]




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