A New Tetrahydrofurannulation Via Tandem Radical Cyclization Reaction-Reductive Deoxygenation Sequence
| Data(s) |
13/02/1995
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|---|---|
| Resumo |
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. |
| Formato |
application/pdf |
| Identificador |
http://eprints.iisc.ernet.in/19260/1/1.pdf 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. |
| Publicador |
Elsavier |
| Relação |
http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THS-40GSDRJ-1T7-3&_cdi=5290&_user=512776&_orig=search&_coverDate=02%2F13%2F1995&_sk=999639992&view=c&wchp=dGLzVtz-zSkzk&md5=f9ffb0870acccf32ac42cb5d74b1e7f1&ie=/sdarticle.pdf http://eprints.iisc.ernet.in/19260/ |
| Palavras-Chave | #Organic Chemistry |
| Tipo |
Journal Article PeerReviewed |
