| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5288333 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
Four allylic dioxolanes were prepared and reacted with several dienes in the presence of Lewis acids, affording [4+3] cycloadducts. The reaction could be conducted with catalytic amounts of Lewis acid. The use of a chiral Lewis acid gave a cycloadduct with only a low enantiomeric excess.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![[4+3] Cycloadditions of some allylic dioxolanes](/preview/png/5288333.png "First Page Preview: [4+3] Cycloadditions of some allylic dioxolanes")
Authors
Michael Harmata, James A. III, Charles L. Barnes,