A novel double deprotection-peptide cyclisation procedure and its application to the synthesis of analogues of the cyclic tetrapeptide HC-toxin.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Analogs of the cytostatic and antimitogenic agents chlamydocin and HC-toxin: synthesis and biological activity of chloromethyl ketone and diazomethyl ketone-functionalized cyclic tetrapeptides
2. Chemical Constitution of the Host-Specific Toxin of Helminthosporium carbonum
3. Amino Acid Composition of the Host-specific Toxin of Helminthosporium carbonum
4. Reciprocal biological activities of the cyclic tetrapeptides chlamydocin and HC-toxin
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1. Total Synthesis of the Naturally Occurring Cyclic Tetrapeptide JM‐47and Analogues through Late‐Stage Functionalization of a Common Scaffold;European Journal of Organic Chemistry;2024-05-22
2. Synthesis of HC-Toxin via Matteson Homologation and C–H Functionalization;The Journal of Organic Chemistry;2023-07-13
3. The Dependence of Endopeptolysis on the Sequential Chirality Exemplified by a Simplified Preparation of the |D-MePhe−4| -Epimer of Virginiamycin s.;Bulletin des Sociétés Chimiques Belges;2010-09-01
4. Simultaneous Use of N-Fmoc and OTmse Protective Groups in the Synthesis of Peptolytic Sensitive Peptides;Bulletin des Sociétés Chimiques Belges;2010-09-01
5. Bop-Cl mediated cyclization of a linear precursor of virginiamycin S. Contra indication for using HOBt as racemization suppressor;Bulletin des Sociétés Chimiques Belges;2010-09-01
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