Synthesis of protected norcysteines for SPPS compatible with Fmoc strategy

We report the synthesis of racemic Alloc-Ncy(Tmob)–OH, the resolution of its methyl ester and demonstrate its application to form a norcystine bridge in octreotide-amide using the Fmoc strategy on solid phase. N-Alloc and S-Tmob protections of norcysteine (Ncy) were found to be a preferred choice fo...

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Veröffentlicht in:Tetrahedron letters 2007-07, Vol.48 (29), p.5107-5110
Hauptverfasser: Samant, Manoj P., Rivier, Jean E.
Format: Artikel
Sprache:eng
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Zusammenfassung:We report the synthesis of racemic Alloc-Ncy(Tmob)–OH, the resolution of its methyl ester and demonstrate its application to form a norcystine bridge in octreotide-amide using the Fmoc strategy on solid phase. N-Alloc and S-Tmob protections of norcysteine (Ncy) were found to be a preferred choice for Fmoc strategy over three other protected norcysteines synthesized, that is, Fmoc-Ncy( tBu)–OH, Alloc-Ncy( tBu)–OH, and Alloc-Ncy(Trt)–OH.
ISSN:0040-4039
1873-3581
DOI:10.1016/j.tetlet.2007.05.082