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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
Journal: Tetrahedron Letters Volume 56, Issue 36, 1 August 2015, Pages 5082-5085 
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.
DOI: 10.1016/j.tetlet.2015.07.042
Appears in Collections:COE Scholarly Publication

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