| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277093 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
Photoinduced electron transfer catalyzed ring opening of aryl-substituted oxiranecarbonitriles via Cβ-O bond cleavage was achieved using 2,4,6-triphenylpyrylium tetrafluoroborate (TPT) as a sensitizer and subsequent [3+2] cycloaddition reaction with electron-rich olefins afforded polysubstituted tetrahydrofurans in good to moderate yields.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jinhui Pan, Wei Zhang, Jie Zhang, Shenci Lu,
![First Page Preview: Photochemically catalyzed ring opening of oxiranecarbonitriles and [3+2] cycloaddition with olefins: synthesis of polysubstituted tetrahydrofurans Photochemically catalyzed ring opening of oxiranecarbonitriles and [3+2] cycloaddition with olefins: synthesis of polysubstituted tetrahydrofurans](/preview/png/5277093.png)