
Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/2722
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DC Field | Value | Language |
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dc.contributor.author | Dhiman, Seema | - |
dc.contributor.author | Ramasastry, S.S.V. | - |
dc.date.accessioned | 2020-12-07T06:18:26Z | - |
dc.date.available | 2020-12-07T06:18:26Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | Organic and Biomolecular Chemistry,11(46),pp.8030-8035. | en_US |
dc.identifier.other | https://doi.org/10.1039/C3OB41945B | - |
dc.identifier.uri | https://pubs.rsc.org/en/content/articlelanding/2013/ob/c3ob41945b#!divAbstract | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2722 | - |
dc.description.abstract | An efficient synthetic approach to diheteroarylmethanes and 1,3-diheteroarylpropenes has been developed via Yb(III)-catalyzed sequential self-condensation of 2-furfuryl (or 2-thienyl or 3-indolyl) alcohols followed by intramolecular Friedel–Crafts type reaction and elimination of an aldehyde. This method offers a powerful entry and a potential alternative to the traditional synthesis of diheteroarylalkanes, which are precursors to the synthesis of several intriguing heteroaryls and more significantly, to the synthesis of biofuels. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.subject | Efficient | en_US |
dc.subject | Synthetic approach | en_US |
dc.subject | Alcohols | en_US |
dc.title | Di- and triheteroarylalkanes via self-condensation and intramolecular Friedel–Crafts type reaction of heteroaryl alcohols† | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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