Synthesis of Acidiphilamide A–C: Secondary Metabolites from the Genus Streptacidiphilus
We describe the efficient total syntheses of naturally occurring tripeptides acidiphilamides A–C and epi-acidiphilamides A–C, which were prepared from commercially available l-phenyl alanine using hexafluorophosphate azabenzotriazole tetramethyl uronium (HATU) as peptide coupling reagent. The structures of the natural acidiphilamides A, B and C were characterized by NMR, MS and SOR data, which match those of natural products, whereas the structures of epi-acidiphilamides A, B and C were confirmed by 2D NMR studies.
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Synthesis of Acidiphilamide A–C: Secondary Metabolites from the Genus Streptacidiphilus ; volume:07 ; number:01 ; year:2023 ; pages:130-139
SynOpen ; 07, Heft 01 (2023), 130-139
- Contributor
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Mallesham, Poosa
Raghavulu, Karri
Miriyala, Venkatesh
Doddipalla, Raju
Yennam, Satyanarayana
Sanasi, Paul Douglas
Behera, Manoranjan
- DOI
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10.1055/a-2035-9753
- URN
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urn:nbn:de:101:1-2023051111025369248804
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:44 AM CEST
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Mallesham, Poosa
- Raghavulu, Karri
- Miriyala, Venkatesh
- Doddipalla, Raju
- Yennam, Satyanarayana
- Sanasi, Paul Douglas
- Behera, Manoranjan
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