A new route to ring-fused tetrahydrofurans: reaction of Δ4-unsaturated alcohols with phenylselenenyl chloride
- 15 November 1977
- journal article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 55 (22) , 3894-3897
- https://doi.org/10.1139/v77-551
Abstract
Δ4-Olefinic alcohols react with phenylselenenyl chloride to produce tetrahydrofurans with a phenylseleno-group trans and β to the ether oxygen. The [4.3.0] and [3.3.0] oxabicyclic systems produced have cis ring fusion as in 5 and 7.Keywords
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