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Synthesis of aza-analogues of the glycosylated tyrosine portion of Mannopeptimycin-E
Two C4’ amido disaccharide analogues of mannopeptimycin-E were synthesized via an iterative palladium glycosylation sequence. The stereoselective synthesis of the C4’ acylated 1,4-α,α-manno,manno-amido disaccharide has been achieved in ten steps from a protected D-tyrosine. The path relies upon a re...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2546506/ https://ncbi.nlm.nih.gov/pubmed/17530803 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo070326r |
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