Formation of aminosuccinyl derivative from β-phenacyl aspartyl peptides catalyzed by sodium thiophenoxide
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1982.tb03039.x/fullpdf
Reference12 articles.
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4. Studies on peptides. 68. Synthesis of the tritriacontapeptide amide corresponding to the entire amino acid sequence of the desulfated form of porcine cholecystokinin-pancreozymin (CCK-PZ).
5. Physalaemin-analoga-synthesen am festen träger
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. An efficient method for the synthesis of phenacyl ester-protected dipeptides using neutral alumina-supported sodium carbonate ‘Na2CO3/n-Al2O3’;Journal of Peptide Science;2013-08-28
2. Allyl ester as temporary protecting group for the β-carboxy function of aspartic acid;International Journal of Peptide and Protein Research;2009-01-12
3. Cleavage of aspartyl β-phenacyl esters by selenophenol under neutral conditions;International Journal of Peptide and Protein Research;2009-01-12
4. New enzymatic approach to the synthesis of convenient aspartic acid intermediates in peptide chemistry. Synthesis of n-benzyloxycarbonyl-l-aspartic acid β-allyl ester.;Tetrahedron;1989-01
5. ChemInform Abstract: FORMATION OF AMINOSUCCINYL DERIVATIVE FROM β-PHENACYL ASPARTYL PEPTIDES CATALYZED BY SODIUM THIOPHENOXIDE;Chemischer Informationsdienst;1982-07-06
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