Journal
CHEMISTRY-A EUROPEAN JOURNAL
Volume 18, Issue 38, Pages 12020-12027Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201201219
Keywords
amination; copper; dicarbonyl compounds; homogenous catalysis; iminoiodanes
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Funding
- University Research Committee Grant from Nanyang Technological University (NTU) [RG55/06]
- Nanyang President's Graduate Scholarship
- Undergraduate Research Experience on Campus stipend from NTU
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A method to prepare a,a-acyl amino acid derivatives efficiently by Cu(OTf)2+1,10-phenanthroline (1,10-phen)-catalyzed amination of 1,3-dicarbonyl compounds with PhI?NSO2Ar is described. The mechanism is thought to initially involve aziridination of the enolic form of the substrate, formed in situ through coordination to the Lewis acidic metal catalyst, by the putative coppernitrene/imido species generated from the reaction of the metal catalyst with the iminoiodane source. Subsequent ring opening of the resultant aziridinol adduct under the Lewis acidic conditions then provided the a-aminated product. The utility of this method was exemplified by the enantioselective synthesis of a precursor of 3-styryl-2-benzoyl-L-alanine.
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