Utilizing Proline Surrogates in the Synthesis of ‘Difficult’ Peptides
Contributors: Hisashi Yamamoto, Alex Boateng
Significance
The synthesis of complex peptides with sequences that readily aggregate remains a huge challenge even with conventional methods. Herein, the authors report an efficient strategy to access them.
Comment
A variety of novel 2-(oxazolidine-2-yl)phenol compounds were produced as proline surrogates and utilized in accessing ‘difficult’ peptides such as thymosin α1.
Wang X, Jin K. Shandong University, Jinan, P. R. of China
Robust Chemical Synthesis of “Difficult Peptides” via 2-Hydroxyphenol-pseudoproline (ψ2-hydroxyphenolpro) Modifications.
J. Org. Chem. 2024; 89: 3143-3149
DOI: 10.1021/acs.joc.3c02576.
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