Abstract
Optimized selective S-acylations of cysteine esters gave intermediates for the synthesis of macrocyclic peptoids by a benzotriazole-based method. © Georg Thieme Verlag Stuttgart · New York.
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APA
Ibrahim, M. A., Panda, S. S., Nhon, L., Hamed, A., El-Feky, S. A., & Katritzky, A. R. (2013). Macrocyclic peptoids by selective s-acylation of cysteine esters. Synthesis (Germany), 45(6), 767–772. https://doi.org/10.1055/s-0032-1318148
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