Phenylthiocarbamate or N-Carbothiophenyl Group Chemistry in Peptide Synthesis and Bioconjugation
Author:
Affiliation:
1. UMR CNRS 8161, F-59021 Lille, France
2. Pasteur Institute of Lille, F-59021 Lille, France
3. Univ Lille Nord de France, F-59000 Lille, France
4. UDSL, EA 4481, UFR Pharmacie, F-59000 Lille, France
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology
Link
https://pubs.acs.org/doi/pdf/10.1021/bc500052r
Reference104 articles.
1. Rapid and selective reduction of functionalized aromatic disulfides with lithium tri-tert-butoxyaluminohydride. A remarkable steric and electronic control. Comparison of various hydride reagents
2. Phenyl-thio-carbonyl Chloride as a Group-protecting Agent
3. The synthesis of peptides related to gramicidin S and the significance of optical configuration in antibiotic peptides. 2. Pentapeptides
4. Studies on Polypeptides. IV.1 Remarks Regarding the Use of the Phenylthiocarbonyl Protecting-group in Peptide Synthesis
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