Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10571699 | Inorganica Chimica Acta | 2005 | 10 Pages |
Abstract
Mild and rapid methanolysis of the terpyridine-appended amide substrate proceeded via its Cu2+ complex in the presence of Cu2+ in methanol or aqueous methanol at 30 °C. The reactivity of the complex was changed according to protonation states of the amide and α-amino group of the complex. The complex having “deprotonated-amide” and “non-protonated α-amino group” exhibited the highest reactivity.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Satoshi Kawaguchi, Koji Araki,