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 |
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Hauptverfasser: | , |
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. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2007.05.082 |