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 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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•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. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2020.152560 |