Application of the 2-adamantyloxycarbonyl (2-adoc) group to the protection of the imidazole function of histidine in peptide synthesis
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1994/C3/C39940002515
Cited by 5 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. Amino acid deletion products resulting from incomplete deprotection of the Boc group fromNπ-benzyloxymethylhistidine residues during solid-phase peptide synthesis;Journal of Peptide Science;2005
2. 2-Adamantyl Chloroformate;Encyclopedia of Reagents for Organic Synthesis;2003-10-15
3. On the allyl protection of the imidazole ring of histidine;Tetrahedron;1997-09
4. The Nim-(2,4-dimethylpent-3-yloxycarbonyl)(Doc) group, a new nucleophile-resistant, HF-cleavable protecting group for histidine in peptide synthesis;Chem. Commun.;1996
5. Amino acids and peptides. Part 42. Application of the 2-adamantyloxycarbonyl (2-Adoc) group to the protection of the imidazole function of histidine in peptide synthesis;Journal of the Chemical Society, Perkin Transactions 1;1995
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