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Total Synthesis of (±)-Cephalosol via Silyl Enol Ether Acylation
| Content Provider | Scilit |
|---|---|
| Author | Koert, Ulrich Arlt, Alexander |
| Copyright Year | 2010 |
| Description | An efficient total synthesis of (±)-cephalosol is reported. Key steps are the acylation of a silyl enol ether with monomethyl oxalyl chloride and the subsequent acid-mediated ring closure to the isocoumarin structure. A chemoselective allylation and the conversion of the olefin into a methyl acetate were applied to install the γ-lactone moiety. |
| Related Links | http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0029-1218647.pdf |
| Ending Page | 922 |
| Page Count | 6 |
| Starting Page | 917 |
| ISSN | 00397881 |
| e-ISSN | 1437210X |
| DOI | 10.1055/s-0029-1218647 |
| Journal | Synthesis |
| Issue Number | 06 |
| Volume Number | 2010 |
| Language | English |
| Publisher | Georg Thieme Verlag KG |
| Publisher Date | 2010-01-12 |
| Access Restriction | Open |
| Subject Keyword | Journal: Synthesis Organic Chemistry |
| Content Type | Text |
| Resource Type | Article |
| Subject | Organic Chemistry Catalysis |