非对映选择性 C(sp3)-H-环化实现新一代环烷糖肽的设计

Samir, MESSAOUDI, Sokna , Bazzi, Ameni , Hadj Mohamed, Dmytro , Ryzhakov, Juba , Ghouilem, Mehdi A. , Beniddir, Vincent , Gandon
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引用次数: 0

摘要

在此,我们报告了一条通过选择性 C-H 芳基化异构键合成糖肽的大环化路线。这种方法证明了 Pd 催化 C-H 活化技术在获得陌生环肽方面的强大威力。
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Diastereoselective Anomeric C(sp3)-H Cyclization Towards the Design of New Generations of Cyclophane-Braced Glycopeptides
Here we report a macrocyclization route towards the synthesis of glycophane peptides by a selective C-H arylation of the anomeric bond. This approach demonstrates the power of Pd-catalysis C-H activation to access unfamiliar cyclic peptides
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