Synthesis of small cyclic peptides constrained with 3-(3-aminomethylphenyl) propionic acid linkers using free radical-mediated macrocyclization

dc.contributor.author Balraju, V.
dc.contributor.author Reddy, D. Srinivasa
dc.contributor.author Periasamy, Mariappan
dc.contributor.author Iqbal, Javed
dc.date.accessioned 2022-03-27T09:08:43Z
dc.date.available 2022-03-27T09:08:43Z
dc.date.issued 2005-08-01
dc.description.abstract In this letter, we report that small peptides (di- and tri-) having a 3-bromobenzyl group at the C-termini and an acryloyl group at the N-termini undergo an efficient Bu3SnH-AIBN mediated intramolecular free radical cyclization to afford cyclic peptides in good yields. We also propose that these cyclizations are occurring via a pre-organized acyclic structure dictated by a reverse turn (γ/β-turn).
dc.identifier.citation Tetrahedron Letters. v.46(31)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/j.tetlet.2005.05.115
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040403905011731
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12487
dc.subject Cyclic peptide
dc.subject Free radical
dc.subject Peptidomimetics
dc.title Synthesis of small cyclic peptides constrained with 3-(3-aminomethylphenyl) propionic acid linkers using free radical-mediated macrocyclization
dc.type Journal. Article
dspace.entity.type
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