Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/99536
Title: Copper(II) Triflate catalyzed amination of 1,3-dicarbonyl compounds
Authors: Ton, Thi My Uyen
Himawan, Fanny
Chang, Joyce Wei Wei
Chan, Philip Wai Hong
Issue Date: 2012
Source: Ton, T. M. U., Himawan, F., Chang, J. W. W.,& Chan, P. W. H. (2012). Copper(II) Triflate Catalyzed Amination of 1,3-Dicarbonyl Compounds. Chemistry - A European Journal, 18(38), 12020-12027.
Series/Report no.: Chemistry - a European journal
Abstract: A method to prepare α,α-acyl amino acid derivatives efficiently by Cu(OTf)2+1,10-phenanthroline (1,10-phen)-catalyzed amination of 1,3-dicarbonyl compounds with PhI[DOUBLE BOND]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 copper–nitrene/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 α-aminated product. The utility of this method was exemplified by the enantioselective synthesis of a precursor of 3-styryl-2-benzoyl-l-alanine.
URI: https://hdl.handle.net/10356/99536
http://hdl.handle.net/10220/12901
ISSN: 0947-6539
DOI: 10.1002/chem.201201219
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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