Srikrishna, A. ; Sundarababu, G. (1990) A radical cyclisation reaction based strategy to 2,3,5-tri- and tetrasubstituted furans Tetrahedron, 46 (23). pp. 7901-7910. ISSN 0040-4020
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/S0040-4020(01)90088-2
Abstract
Synthesis of 2,3,5-trisubstituted furans (5̲), starting from 2-methoxypropene and 1,3-disubstituted propargyl alcohols 3̲ via̲, the radical cyclisation of the bromo acetal 4̲ followed by aromatisation, is reported. Analogously, l-methoxycyclohexene and propargyl alcohols 3̲ furnished the tetrasubstituted furans 6̲.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| ID Code: | 48756 |
| Deposited On: | 15 Jul 2011 11:23 |
| Last Modified: | 15 Jul 2011 11:23 |
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