Semisynthetic Di- and Tri-Functionalized Non-Immunosuppressive Cyclosporin A Derivatives as Potential Anti-HIV 1 Drugs
Abstract A regio- and stereoselective synthesis of original semisynthetic di- and tri-functionalized non-immunosuppressive cyclosporins by way of a Barton ester decarboxylation and a C-thioalkylation starting from cyclosporin A (CsA) and [4′-hydroxy-MeLeu] 4 -CsA is described.
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Veröffentlicht in: | Synlett 2004-02, Vol.2004 (2), p.0316-0320 |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Abstract
A regio- and stereoselective synthesis of original semisynthetic di- and tri-functionalized non-immunosuppressive cyclosporins by way of a Barton ester decarboxylation and a C-thioalkylation starting from cyclosporin A (CsA) and [4′-hydroxy-MeLeu]
4
-CsA is described. |
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ISSN: | 0936-5214 1437-2096 |
DOI: | 10.1055/s-2004-815405 |