Convenient Peptide Synthesis without Protection of C-Terminals
Author:
Affiliation:
1. Faculty of Pharmacy, Chiba Institute of Science
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
http://www.journal.csj.jp/doi/pdf/10.1246/cl.2012.42
Reference8 articles.
1. Amide bond formation and peptide coupling
2. Acylation of unprotected amino acids using ultrasound
3. The Use of Esters of N-Hydroxysuccinimide in Peptide Synthesis
4. Synthesis and in vitro binding of N-phenyl piperazine analogs as potential dopamine D3 receptor ligands
5. Using mixed anhydrides from amino acids and isobutyl chloroformate in N-acylations: a case study on the elucidation of mechanism of urethane formation and starting amino acid liberation using carbon dioxide as the probe
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