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DC Field | Value | Language |
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dc.contributor.author | Tee, J.T. | en_US |
dc.contributor.author | Chee, C.F. | en_US |
dc.contributor.author | Buckle, M.J.C. | en_US |
dc.contributor.author | Lee, V.S. | en_US |
dc.contributor.author | Chong, W.L. | en_US |
dc.contributor.author | Khaledi, H. | en_US |
dc.contributor.author | Rahman, N.A. | en_US |
dc.date.accessioned | 2017-10-27T06:14:27Z | - |
dc.date.available | 2017-10-27T06:14:27Z | - |
dc.date.issued | 2015 | - |
dc.description.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. | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Tetrahedron Letters Volume 56, Issue 36, 1 August 2015, Pages 5082-5085 | en_US |
dc.title | Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels-Alder adducts morusalbanol A and 441772-64-1 | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1016/j.tetlet.2015.07.042 | - |
item.grantfulltext | open | - |
item.fulltext | With Fulltext | - |
crisitem.author.dept | Universiti Tenaga Nasional | - |
Appears in Collections: | COE Scholarly Publication |
Files in This Item:
File | Size | Format | |
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Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels-Alder adducts morusalbanol A and 441772-64-1.pdf | 821.91 kB | Adobe PDF | View/Open |
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