| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5261224 | Tetrahedron Letters | 2014 | 4 Pages |
Abstract
A convenient, two-step synthesis of substituted furans from readily available aryl alkynes and ketones is reported. The furan-forming oxidative cyclization is mediated by the combination of cerium(IV) ammonium nitrate and potassium bromide and can be carried out in an open flask.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Sridhar Undeela, Joshi P. Ramchandra, Rajeev S. Menon,
