Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5216525 | Tetrahedron | 2014 | 6 Pages |
Abstract
Ring-closing metathesis is commonly utilized in peptide macro-cyclization. The influence of α-methylation of the amino acids bearing the olefin moieties has never been systematically studied. In this report, controlled reactions unambiguously indicate that α-methylation at the N-terminus of the metathesis sites is crucial for this reaction to occur. Also, we first elucidated that the E-isomers of stapled peptides are significantly more helical than the Z-isomers.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Qingzhou Zhang, Xiaodong Shi, Yanhong Jiang, Zigang Li,