| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279730 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
The 2,3-bis(spiro-2-indanyl-1,3-dione)-indeno[1,2-b]furan-4-one has been synthesized by cathodic reduction of 2,2-dibromo-1,3-indandione in dichloromethane-Bu4NBF4. In contrast, tris-indanedione was the main product when acetonitrile was used as a solvent. Sunlight exposition of the dispiro compound afforded the tris-indandione in quantitative yield.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
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