Mild, rapid and selective alcoholysis of terpyridine-appended amide substrates by Cu2+-catalysis: Protonation state and reactivity of the complex

Inorganica Chimica Acta

Volumn 358, Issue 4, 2005, Pages 947-956

  Kawaguchi, Satoshi ^a,b   Araki, Koji ^a  

^a INSTITUTE OF INDUSTRIAL SCIENCE   (Japan)

^b Technical Research Institute   (Japan)

Author keywords

Amide alcoholysis; Aminoacylation; Copper complexes; Highly reactive amide bond; Protonation states; Terpyridine appended amide

Indexed keywords

AMIDES; AMINO ACIDS; METAL COMPLEXES; METHANOL; PROTONATION; RATE CONSTANTS; SUBSTRATES;

ALCOHOLYSIS; AMIDE BOND; AMINOACYLATION; COPPER COMPLEXES; PROTONATION STATE; TERPYRIDINES;

COPPER COMPOUNDS;

AMIDE; AMMONIA; CARBONYL DERIVATIVE; COPPER; METAL COMPLEX; METHANOL; NITROGEN; PHENYLALANINE METHYL ESTER; PYRIDINE;

ALCOHOLYSIS; ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; COMPLEX FORMATION; PROTON TRANSPORT; REACTION ANALYSIS; TEMPERATURE; TITRIMETRY;

EID: 13844308665     PISSN: 00201693     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ica.2004.10.008     Document Type: Article

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