Critical examination of a method for the analysis of .alpha. and .omega. linkages in peptides containing aspartic acid and glutamic acid
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00160a015
Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Synthesis of imidazolidin-2-one-4-carboxylate and of (tetrahydro)pyrimidin-2-one-5-carboxylate via an efficient modification of the Hofmann rearrangement;Organic & Biomolecular Chemistry;2008
2. Selective Peptide Chain Extension at the C-terminus of Aspartic and Glutamic Acids Utilizing N-protected (α-aminoacyl)benzotriazoles;Chemical Biology Drug Design;2006-07
3. A new type of safety-catch linker cleaved by intramolecular activation of an amide anchorage and allowing aqueous processing in solid-phase peptide synthesis;Journal of the Chemical Society, Chemical Communications;1993
4. Structure determination of lysobactin, a macrocyclic peptide lactone antibiotic;The Journal of Organic Chemistry;1989-03
5. Distinction of α- and β-aspartyl and α- and γ-glutamyl peptides by fast atom bombardment/tandem mass spectrometry;Biological Mass Spectrometry;1988-04-01
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