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Chemistry ; 19(40): 13309-12, 2013 Sep 27.
Article in English | MEDLINE | ID: mdl-24027163

ABSTRACT

Significant differences in the reactivity of norbornene derivatives in the inverse electron-demand Diels-Alder reaction with tetrazines were revealed by kinetic studies. Substantial rate enhancement for the exo norbornene isomers was observed. Quantum-chemical calculations were used to rationalize and support the observed experimental data.


Subject(s)
Anhydrides/chemistry , Norbornanes/chemistry , Cycloaddition Reaction , Electrons , Kinetics , Molecular Structure , Quantum Theory
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