Synthesis of unnatural amino acids functionalized with sterically shielded pyrroline nitroxides

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Abstract

A series of unnatural amino acids functionalized with sterically shielded pyrroline nitroxides were synthesized. Their reduction by ascorbate/glutathione indicates that L-cysteine functionalized with gem-diethylpyrroline nitroxide is reduced at the slowest rate and is comparable to that measured for the most resistant to reduction pyrroline and pyrrolidine nitroxides. (Chemical Equation Presented).

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Wang, Y., Paletta, J. T., Berg, K., Reinhart, E., Rajca, S., & Rajca, A. (2014). Synthesis of unnatural amino acids functionalized with sterically shielded pyrroline nitroxides. Organic Letters, 16(20), 5298–5300. https://doi.org/10.1021/ol502449r

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