Please use this identifier to cite or link to this item: http://dspace2020.uniten.edu.my:8080/handle/123456789/9735
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dc.contributor.authorTee, J.T.
dc.contributor.authorChee, C.F.
dc.contributor.authorBuckle, M.J.C.
dc.contributor.authorLee, V.S.
dc.contributor.authorChong, W.L.
dc.contributor.authorKhaledi, H.
dc.contributor.authorRahman, N.A.
dc.date.accessioned2018-03-06T03:49:14Z-
dc.date.available2018-03-06T03:49:14Z-
dc.date.issued2015
dc.identifier.urihttp://dspace.uniten.edu.my/jspui/handle/123456789/9735-
dc.description.abstractPreparation of the oxabicyclic [3.3.1] cores of morusalbanol A and 441772-64-1 was achieved via the intramolecular cyclization of cis-trans (endo) mulberry Diels-Alder adducts. The latter were derived from a hydrogen bond-assisted regioselective Diels-Alder reaction between a chalcone dienophile and a dehydroprenyl diene. Results from these studies provide important insights into the syntheses of morusalbanol A and related mulberry Diels-Alder adducts. © 2015 Elsevier Ltd. All rights reserved.
dc.titleModel studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels-Alder adducts morusalbanol A and 441772-64-1
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptUniversiti Tenaga Nasional-
Appears in Collections:COE Scholarly Publication
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