| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5266695 | Tetrahedron Letters | 2016 | 10 Pages |
Abstract
A total synthesis of the unusual naturally occurring 2,4-disubstituted pyrrole, Pyrrolostatin, is described, which features formation of the central pyrrole ring by a silver(I)-catalysed 5-endo-dig cyclisation.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Damian G. Dunford, David W. Knight,