Please use this identifier to cite or link to this item:
|Title:||Synthesis of (±)-kuwanon v and (±)-dorsterone methyl ethers via Diels-Alder reaction||Authors:||Chee, C.F.
|Issue Date:||2011||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.||URI:||http://dspace.uniten.edu.my/jspui/handle/123456789/9792|
|Appears in Collections:||COE Scholarly Publication|
Show full item record
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.