| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278027 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
Cycloaddition of 3-O-allyl-1,2-isopropylidene N-Ph nitrones afforded appreciably increased yields of oxepanes compared to the corresponding N-Me or N-Bn nitrones. Higher yields permitted some useful further transformations of the oxepanes.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Seema Datta, Madhumita Nath, Sandip Chowdhury, Anup Bhattacharjya,