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dc.contributor.authorTee, J.T.en_US
dc.contributor.authorChee, C.F.en_US
dc.contributor.authorBuckle, M.J.C.en_US
dc.contributor.authorLee, V.S.en_US
dc.contributor.authorChong, W.L.en_US
dc.contributor.authorKhaledi, H.en_US
dc.contributor.authorRahman, N.A.en_US
dc.date.accessioned2017-10-27T06:14:27Z-
dc.date.available2017-10-27T06:14:27Z-
dc.date.issued2015-
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.en_US
dc.language.isoenen_US
dc.relation.ispartofTetrahedron Letters Volume 56, Issue 36, 1 August 2015, Pages 5082-5085en_US
dc.titleModel studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels-Alder adducts morusalbanol A and 441772-64-1en_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.tetlet.2015.07.042-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.languageiso639-1en-
crisitem.author.deptUniversiti Tenaga Nasional-
Appears in Collections:COE Scholarly Publication
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