Advanced Synthesis & Catalysis · 2012 · 62 citations · 88 references
Natural SciencesChemistryMedicinal ChemistryCatalysisNatural Product BiosynthesisOrganic ChemistryCatalyst PreparationOrganic SynthesisChiral Product SynthesisEnantioselective CatalysisEnantioselective ReductionEnantioselective SynthesisIndole ChemistryIndole DerivativesIndole SynthesisMild Reaction Conditions
Abstract A new strategy for the synthesis of N‐alkoxycarbonyl aryl α‐imino esters in the presence of dirhodium tetraacetate [Rh 2 (OAc) 4 ] is reported to produce the desired compounds in high yield (up to 96%) under mild reaction conditions. The application of the synthetic method is demonstrated in enantioselective reduction and Friedel–Crafts reaction of indoles to afford the corresponding chiral arylglycines and indole derivatives, respectively, in high yield and excellent ee .
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Recent studies on the reactions of α-diazocarbonyl compounds
Zhenhua Zhang, Jianbo Wang · Tetrahedron · 2008 · 765 citations
Enantioselective Organocatalytic Reductive Amination
Richard Storer, Diane E. Carrera, Yike Ni et al. · Journal of the American Chemical Society · 2005 · 731 citations