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The kinetics of the reactions of various primary and secondary amines with the benzhydrylium ions in water are investigated, demonstrating their nucleophilcites. The results show a poor correlation between the nucleophilicities values, as the secondary alkyl amines and anilines are more nucleophilicdue to the difference in their pH values.

The reactions of N-chlorotaurine with several nucleophilic reagents, the protonation at nitrogen during the transfer of chlorine from N-chlorotaurine to a nucleophile and its mechanisms of transfer reactions are studied. The results have provided evidence against an electron-transfer mechanism for chlorination of the nuclophiles by protonated N-chlorotaurine.

A study conducted reports that triflyl azide rapidly reacts with a series of amine-functionalized solid supports to generate azide-coated supports. The results show that the so-formed azide coat could be used to load leader nucleoside monomers on solid supports using click chemistry under benign experimental conditions.

The reactivity of (2-azaallyl)nitriles toward double nucleophilic addition and the double allylation reactions of (2-azaallyl)stannanes are reported. The conversion of the N,N-bis(3-butenyl)amines obtained as products from the double allylation reactions to 2,3,6,7-tetrahydroazepines through ring-closing metathesis is described.