dc.contributor.author | Jacobsen, Eric N. | |
dc.contributor.author | Beck, Elizabeth M. | |
dc.contributor.author | Hyde, Alan M. | |
dc.date.accessioned | 2012-05-14T18:12:14Z | |
dc.date.issued | 2011 | |
dc.identifier.citation | Beck, Elizabeth M., Alan M. Hyde, and Eric N. Jacbosen. 2011. Chiral sulfinamide/achiral sulfonic acid cocatalyzed enantioselective protonation of enol silanes. Organic Letters 13(16): 4260-4263. | en_US |
dc.identifier.issn | 1523-7060 | en_US |
dc.identifier.uri | http://nrs.harvard.edu/urn-3:HUL.InstRepos:8737993 | |
dc.description.abstract | The application of chiral sulfinamides and achiral sulfonic acids as a co-catalyst system for enantioselective protonation reactions is described. Structurally simple, easily accessible sulfinamides were found to induce moderate-to-high eeʼs in the formation of 2-aryl-substituted cycloalkanones from the corresponding trimethylsilyl enol ethers. | en_US |
dc.description.sponsorship | Chemistry and Chemical Biology | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | American Chemical Society | en_US |
dc.relation.isversionof | doi:10.1021/ol201608a | en_US |
dc.relation.hasversion | https://www.ncbi.nlm.nih.gov/pubmed/21786775 | en_US |
dash.license | OAP | |
dc.subject | polyphenyl derivatives | en_US |
dc.subject | diastereoselective syntheses | en_US |
dc.subject | enantioselective syntheses | en_US |
dc.subject | cycloalkylphenyl derivatives | en_US |
dc.title | Chiral Sulfinamide/Achiral Sulfonic Acid Cocatalyzed Enantioselective Protonation of Enol Silanes | en_US |
dc.type | Journal Article | en_US |
dc.description.version | Author's Original | en_US |
dc.relation.journal | Organic Letters | en_US |
dash.depositing.author | Jacobsen, Eric N. | |
dc.date.available | 2012-05-14T18:12:14Z | |
dc.identifier.doi | 10.1021/ol201608a | * |
dash.authorsordered | false | |
dash.contributor.affiliated | Jacobsen, Eric | |