Please use this identifier to cite or link to this item: http://dspace2020.uniten.edu.my:8080/handle/123456789/9735
Title: Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels-Alder adducts morusalbanol A and 441772-64-1
Authors: Tee, J.T.
Chee, C.F.
Buckle, M.J.C.
Lee, V.S.
Chong, W.L.
Khaledi, H.
Rahman, N.A.
Issue Date: 2015
Abstract: Preparation 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.
URI: http://dspace.uniten.edu.my/jspui/handle/123456789/9735
Appears in Collections:COE Scholarly Publication

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