A new photoclick reaction strategy: Photo-induced catalysis of the thiol-Michael addition via a caged primary amine

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Abstract

The utilization of 2-(2-nitrophenyl)propyloxycarbonyl (NPPOC) as a photolabile primary amine cage enables the thiol-Michael ‘click’ reaction to be photo-triggered. The photolabile amine exhibits efficient catalytic activity upon UV irradiation and is shown to initiate the photopolymerization of tetrathiol and diacrylate comonomers via Michael addition. © 2013 The Royal Society of Chemistry.

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Xi, W., Krieger, M., Kloxin, C. J., & Bowman, C. N. (2013). A new photoclick reaction strategy: Photo-induced catalysis of the thiol-Michael addition via a caged primary amine. Chemical Communications, 49(40), 4504–4506. https://doi.org/10.1039/c3cc41123k

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