| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5288310 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
An efficient and highly diastereoselective preparation of highly substituted tetrahydrofurans from the cyclocondensation of vicinal t-butyldiphenylsilylmethyl-substituted cyclopropyl diesters with aldehydes and ketones has been developed.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![A highly diastereoselective approach to tetrahydrofurans via [3+2] cycloadditions of silylmethyl-substituted cyclopropanes with aldehydes and ketones](/preview/png/5288310.png "First Page Preview: A highly diastereoselective approach to tetrahydrofurans via [3+2] cycloadditions of silylmethyl-substituted cyclopropanes with aldehydes and ketones")
Authors
Archana Gupta, Veejendra K. Yadav,