A facile synthesis of meta- and para-terphenylglyoxamide-based peptidomimetics

[Display omitted] •A simple and efficient procedure for thesynthesis of meta- and para-substituted terphenyl compounds.•A facile synthesis of novel 5-biphenyl substituted N-acylisatins.•Versatile and robust synthesis of terphenylglyoxamides under mild conditions. A series of meta- and para-terphenyl...

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Veröffentlicht in:Tetrahedron letters 2020-11, Vol.61 (48), p.152560, Article 152560
Hauptverfasser: Yu, Tsz Tin, Bhadbhade, Mohan, Kuppusamy, Rajesh, Black, David StC, Kumar, Naresh
Format: Artikel
Sprache:eng
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Zusammenfassung:[Display omitted] •A simple and efficient procedure for thesynthesis of meta- and para-substituted terphenyl compounds.•A facile synthesis of novel 5-biphenyl substituted N-acylisatins.•Versatile and robust synthesis of terphenylglyoxamides under mild conditions. A series of meta- and para-terphenylglyoxamide peptidomimetics have been synthesised by the ring-opening of 5-(biphenylyl)-N-acylisatins with alcohols, amines and amino acid methyl esters. The starting 5-(biphenylyl)isatins were synthesised via the Suzuki-Miyaura coupling reaction in a convenient and efficient manner.
ISSN:0040-4039
1873-3581
DOI:10.1016/j.tetlet.2020.152560