Publication | Closed Access
Vicinal Amino Alcohols as Organocatalysts in Asymmetric Cross-Aldol Reaction of Ketones: Application in the Synthesis of Convolutamydine A
181
Citations
24
References
2007
Year
Convolutamydine ATransition StateNovel OrganocatalystsEnantioselective SynthesisBiochemistryOrganic ChemistryVicinal Amino AlcoholsAsymmetric Cross-aldol ReactionUncommon Mechanistic FeaturesStereoselective SynthesisPharmacologyAsymmetric CatalysisSynthetic ChemistryEfficient OrganocatalystsNatural Product Synthesis
Leucinol and valinol have been identified as efficient organocatalysts for the aldol reaction of isatin and its derivatives (as examples of activated, non-enolizable ketones) with acetone. Uncommon mechanistic features were observed and used in the formulation of the transition state of the reaction.
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