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http://dspace2020.uniten.edu.my:8080/handle/123456789/9792Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Chee, C.F. | |
| dc.contributor.author | Lee, Y.K. | |
| dc.contributor.author | Buckle, M.J.C. | |
| dc.contributor.author | Rahman, N.A. | |
| dc.date.accessioned | 2018-03-06T03:49:45Z | - |
| dc.date.available | 2018-03-06T03:49:45Z | - |
| dc.date.issued | 2011 | |
| dc.identifier.uri | http://dspace.uniten.edu.my/jspui/handle/123456789/9792 | - |
| dc.description.abstract | The mulberry Diels-Alder adducts, the pentamethyl ethers of kuwanon V 1a and dorsterone 2a were synthesised via a biomimetic intermolecular [4+2] cycloaddition reaction between a highly electron-rich dienophile and a Lewis acid sensitive diene derived from chalcone. Cycloaddition under thermal conditions afforded 1a and 2a (in 3:2 ratio). Cycloaddition catalysed by AgOTf/Bu4NBH4 gave higher yields of the adducts. © 2010 Elsevier Ltd. All rights reserved. | |
| dc.title | Synthesis of (±)-kuwanon v and (±)-dorsterone methyl ethers via Diels-Alder reaction | |
| item.fulltext | No Fulltext | - |
| item.grantfulltext | none | - |
| crisitem.author.dept | Universiti Tenaga Nasional | - |
| Appears in Collections: | COE Scholarly Publication | |
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