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Site-Selective C(sp(3))–H Functionalization of Di-, Tri-, and Tetrapeptides at the N-Terminus

[Image: see text] Although the syntheses of novel and diverse peptides rely mainly on traditional coupling using unnatural amino acids, postsynthetic modification of peptides could provide a complementary method for the preparation of nonproteinogenic peptides. Site selectivity of postsynthetic modi...

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Detalles Bibliográficos
Autores principales: Gong, Wei, Zhang, Guofu, Liu, Tao, Giri, Ramesh, Yu, Jin-Quan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4277765/
https://www.ncbi.nlm.nih.gov/pubmed/25384178
http://dx.doi.org/10.1021/ja510233h