Please use this identifier to cite or link to this item:
http://dspace.uniten.edu.my/jspui/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 |
Show full item record
Google ScholarTM
Check
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.