| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279560 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
The hetero-Diels-Alder reactions of enolic ethers generated from methylenation of various esters are described, which allow for the rapid synthesis of various substituted [6,6] aromatic spiroketal skeletons.
Graphical abstractThe hetero-Diels-Alder reactions of enolic ethers generated from methylenation of various esters are described, which allow for the rapid synthesis of various substituted [6,6] aromatic spiroketal skeletons.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Guanglian Zhou, Deping Zheng, Shijun Da, Zhixiang Xie, Ying Li,