Srikrishna, A and Viswajanani, R and Yelamaggad, CV (1995) A New Tetrahydrofurannulation Via Tandem Radical Cyclization Reaction-Reductive Deoxygenation Sequence. In: Tetrahedron Letters, 36 (7). pp. 1127-1128.
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Abstract
Treatment of bromoketals 2, derived from allyl alcohols 1, with tributyltin chloride, sodium cyanoborohydride and AIBN furnishes the tetrahydrofurannulated products 3 via a 5-exo-trig radical cyclisation reaction followed by reductive cleavage of ketal 4.
| Item Type: | Journal Article |
|---|---|
| Publication: | Tetrahedron Letters |
| Publisher: | Elsavier |
| Additional Information: | Copyright of this article belongs to Elsavier. |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 02 Apr 2009 05:27 |
| Last Modified: | 19 Sep 2010 05:27 |
| URI: | http://eprints.iisc.ac.in/id/eprint/19260 |
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