| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278036 | Tetrahedron Letters | 2008 | 5 Pages |
Abstract
A concise route to isoflavans employing a Diels-Alder reaction between o-quinone methide and aryl-substituted enol ethers followed by reductive cleavage of acetals under Lewis acidic conditions is described.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Santosh J. Gharpure, A.M. Sathiyanarayanan, Prasad Jonnalagadda,