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Large-scale synthesis of all stereoisomers of a 2,3-unsaturated C-glycoside scaffold.
| Publication Type | Journal Article |
| Authors | Gerard, B., Marié JC, Pandya BA, Lee MD 4th, Liu H., and Marcaurelle LA |
| Abstract | 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 groups for downstream reactivity. |
| Year of Publication | 2011 |
| Journal | The Journal of organic chemistry |
| Volume | 76 |
| Issue | 6 |
| Pages | 1898-901 |
| Date Published (YYYY/MM/DD) | 2011/03/18 |
| ISSN Number | 0022-3263 |
| DOI | 10.1021/jo1022926 |
| PubMed | http://www.ncbi.nlm.nih.gov/pubmed/21341742?dopt=Abstract |
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