Publication | Closed Access
Chiral 2,2‘-Bipyridine-Type <i>N</i>-Monoxides as Organocatalysts in the Enantioselective Allylation of Aldehydes with Allyltrichlorosilane
179
Citations
28
References
2002
Year
Chiral 2,2Novel OrganocatalystsEngineeringBiochemistrySakurai-hosomi-type AllylationNatural SciencesOrganic ChemistryCatalysisAxial ChiralityChemistryStereoselective SynthesisAnnulated Terpene UnitsAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringEnantioselective Allylation
[reaction: see text] The Sakurai-Hosomi-type allylation of aromatic and heteroaromatic aldehydes can be catalyzed by the new heterobidenate bipyridine monoxide PINDOX with high enantioselectivities. The sterochemical outcome is mainly controlled by the axial chirality in PINDOX, which in turn is determined by the annulated terpene units.
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