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Large-Scale Synthesis of All Stereoisomers of a 2,3-Unsaturated C-Glycoside Scaffold
[Image: see text] All stereoisomers of a highly functionalized 2,3-unsaturated C-glycoside can be accessed in 10–100 g quantities from readily available starting materials and reagents in 3–7 steps. These chiral scaffolds contain three stereogenic centers along with orthogonally protected functional...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2011
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3073442/ https://ncbi.nlm.nih.gov/pubmed/21341742 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo1022926 |
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