| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5281075 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
New thiol-containing auxiliaries were developed for peptide ligation. They were placed at the amidyl N-atom in the second amino acid residue of a peptide fragment. With the new auxiliaries, peptide ligation could be conducted at non-Cys and non-Gly sites. Compared to other recently developed auxiliaries, an important feature of the present design was that the new auxiliaries were generally applicable and readily removable.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Juan Li, Hong-Kui Cui, Lei Liu,