Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5279738 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
Acceleration of Cu(I)-mediated Huisgen 1,3-dipolar cycloaddition (Sharpless 'click reaction') by non-basic histidine derivatives was found. An efficient 'self-activating' click reaction between the azide- and acetylene-containing peptides on the solid-phase has also been achieved by introducing the Nim-benzylhistidine residue on the reacting peptides.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Katsunori Tanaka, Chika Kageyama, Koichi Fukase,