Peptide synthesis by prior thiol capture—V. The scope and control of disulfide interchange during the acyl transfer step
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. New synthetic concepts in organosulfur chemistry. I. New pathway to unsymmetrical disulfides. The thiol-induced fragmentation of sulfenyl thiocarbonates
2. Sulfur-containing polypeptides. XVIII. Unambiguous synthesis of the parallel and antiparallel isomers of some bis-cystine peptides
3. Sulfur-Containing Polypeptides XVII. The S-Carbomethoxysulfenyl Derivatives as a Protective Group for Cysteine
4. Die gezielte Synthese offenkettiger asymmetrischer Cystinpeptide mittels thiol-induzierter Fragmentierung von Sulfenylthiocarbonanten. Insulinfragmente mit intakter Disulfidbrücke A20-B19.
5. The amine capture strategy for peptide bond formation—an outline of progress
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2. Recent trends in Cys- and Ser/Thr-based synthetic strategies for the elaboration of peptide constructs;Chemical Communications;2012
3. Preparations of Boc-Cys(S-Pyr)-OH and Z-Cys(S-Pyr)-OH and their applications in orthogonal coupling of unprotected peptide segments;The Journal of Peptide Research;2009-01-12
4. Resolution of proline acylation problem for thiol capture strategy by use of a chloro-dibenzofuran template;International Journal of Peptide and Protein Research;2009-01-12
5. Building Complex Glycopeptides: Development of a Cysteine-Free Native Chemical Ligation Protocol;Angewandte Chemie International Edition;2006-06-19
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