| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5267585 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
Efficient syntheses of suitably functionalized top and bottom fragments of tetrafibricin are described. The bottom fragment is prepared by two consecutive Kocienski-Julia couplings, while the top fragment synthesis features a dithiane alkylation and a Horner-Wadsworth-Emmons reaction.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Venugopal Gudipati, Dennis P. Curran,