Synthesis of conformationally constrained cyclic peptides using an intramolecular Sonogashira coupling

dc.contributor.author Balraju, V.
dc.contributor.author Srinivasa Reddy, D.
dc.contributor.author Periasamy, Mariappan
dc.contributor.author Iqbal, Javed
dc.date.accessioned 2022-03-27T09:08:39Z
dc.date.available 2022-03-27T09:08:39Z
dc.date.issued 2005-11-11
dc.description.abstract Small peptides having a 3-bromobenzyl group at the C-termini and n-alkynoyl group at the N-termini undergo a smooth copper-free intramolecular Sonogashira coupling reaction to afford the corresponding cyclic peptides in moderate yields. Scope and limitations of this macrocyclization is demonstrated with di-, tri-, and tetrapeptides. © 2005 American Chemical Society.
dc.identifier.citation Journal of Organic Chemistry. v.70(23)
dc.identifier.issn 00223263
dc.identifier.uri 10.1021/jo051412z
dc.identifier.uri https://pubs.acs.org/doi/10.1021/jo051412z
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12485
dc.title Synthesis of conformationally constrained cyclic peptides using an intramolecular Sonogashira coupling
dc.type Journal. Article
dspace.entity.type
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