Solid-Phase Synthesis of Biaryl Cyclic Peptides Containing a Histidine-Phenylalanine Linkage
Author:
Funder
MINECO/FEDER, EU
University of Girona
Publisher
Springer Science and Business Media LLC
Subject
Drug Discovery,Molecular Medicine,Biochemistry,Bioengineering,Analytical Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s10989-019-09877-5.pdf
Reference17 articles.
1. Afonso A, Rosés C, Planas M, Feliu L (2010) Biaryl peptides from 4-iodophenylalanine by solid-phase borylation and Suzuki-Miyaura cross-coupling. Eur J Org Chem. https://doi.org/10.1002/ejoc.200901350
2. Afonso A, Feliu L, Planas M (2011) Solid-phase synthesis of biaryl cyclic peptides by borylation and microwave-assisted intramolecular Suzuki-Miyaura reaction. Tetrahedron 67:2238–2245. https://doi.org/10.1016/j.tet.2011.01.084
3. Bewley C, He H, Williams D, Faulkner D (1996) Aciculitins A − C: cytotoxic and antifungal cyclic peptides from the lithistid sponge aciculites orientalis. J Am Chem Soc 118:4314–4321. https://doi.org/10.1021/ja953628w
4. Cerezo V, Amblard M, Martinez J, Verdié P, Planas M, Feliu L (2008) Solid-phase synthesis of 5-arylhistidines via a microwave-assisted Suzuki-Miyaura cross-coupling. Tetrahedron 64:10538–10545. https://doi.org/10.1016/j.tet.2008.08.077
5. Feliu L, Planas M (2005) Cyclic peptides containing biaryl and biaryl ether linkages. Int J Pept Res Ther 11:53–97. https://doi.org/10.1007/s10989-004-1723-1
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