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REGIOSELECTIVE GLYCOSYLATION: SYNTHESIS OF α-INDOLINE NUCLEOSIDES
Novel indoline ribonucleosides with the α-N-glycoside configuration are synthesized with very high regioselectivity in 90–96% yield, using TMS protected indolines and 2,3-O-(1-methylethylidene)-5-O-(triphenylmethyl)-α/β-d-ribofuranose. The structures of these ribonucleosides were elucidated with X-r...
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| Huvudupphovsmän: | , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2005
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1383618/ https://ncbi.nlm.nih.gov/pubmed/16270659 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1081/NCN-200067398 |
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