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Sterically shielded tetrazoles for a fluorogenic photoclick reaction: tuning cycloaddition rate and product
1Department of Chemistry, State University of New York at Buffalo, Buffalo, New York 14260, USA. qinglin@buffalo.edu.
Abstract:
A panel of sterically shielded tetrazoles with different N-aryl groups were synthesized and subsequently evaluated in the photoinduced tetrazole-alkene cycloaddition reaction. It was found that increase in the HOMO energy of the corresponding nitrile imines leads to a faster cycloaddition reaction along with a red shift in the fluorescence emission of the pyrazoline cycloadduct.
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