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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.
|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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