Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10595744 | Bioorganic & Medicinal Chemistry Letters | 2011 | 4 Pages |
Abstract
We report the discovery of two long-wavelength (365Â nm) photoactivatable diaryltetrazoles through screening a small library of diaryltetrazoles that were designed using a 'scaffold hopping' strategy. A naphthalene-derived tetrazole showed excellent reactivity in the photoinduced cycloaddition reaction with methyl methacrylate under 365Â nm photoirradiation in acetonitrile PBS buffer mixture. Besides, the brightly fluorescent pyrazoline cycloadducts that were formed further increase the potential utility of these new diaryltetrazoles as 'photoclick' reagents and as reporters in biological studies.
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Authors
Zhipeng Yu, Lok Yin Ho, Zhiyong Wang, Qing Lin,