Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels–Alder adducts morusalbanol A and 441772-64-1

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...

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Main Authors: Tee, Jia Ti, Chee, Chin Fei, Buckle, Michael James Christopher, Lee, Vannajan Sanghiran, Chong, Wei Lim, Khaledi, Hamid, Abd Rahman, Noorsaadah
Format: Article
Published: Elsevier 2015
Subjects:
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author Tee, Jia Ti
Chee, Chin Fei
Buckle, Michael James Christopher
Lee, Vannajan Sanghiran
Chong, Wei Lim
Khaledi, Hamid
Abd Rahman, Noorsaadah
author_facet Tee, Jia Ti
Chee, Chin Fei
Buckle, Michael James Christopher
Lee, Vannajan Sanghiran
Chong, Wei Lim
Khaledi, Hamid
Abd Rahman, Noorsaadah
author_sort Tee, Jia Ti
collection UM
description 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.
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spelling um.eprints-146072019-12-23T03:59:17Z http://eprints.um.edu.my/14607/ Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels–Alder adducts morusalbanol A and 441772-64-1 Tee, Jia Ti Chee, Chin Fei Buckle, Michael James Christopher Lee, Vannajan Sanghiran Chong, Wei Lim Khaledi, Hamid Abd Rahman, Noorsaadah QD Chemistry 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. Elsevier 2015-09-02 Article PeerReviewed Tee, Jia Ti and Chee, Chin Fei and Buckle, Michael James Christopher and Lee, Vannajan Sanghiran and Chong, Wei Lim and Khaledi, Hamid and Abd Rahman, Noorsaadah (2015) Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels–Alder adducts morusalbanol A and 441772-64-1. Tetrahedron Letters, 56 (36). pp. 5082-5085. ISSN 0040-4039, DOI https://doi.org/10.1016/j.tetlet.2015.07.042 <https://doi.org/10.1016/j.tetlet.2015.07.042>. http://www.sciencedirect.com/science/article/pii/S0040403915011958 doi:10.1016/j.tetlet.2015.07.042
spellingShingle QD Chemistry
Tee, Jia Ti
Chee, Chin Fei
Buckle, Michael James Christopher
Lee, Vannajan Sanghiran
Chong, Wei Lim
Khaledi, Hamid
Abd Rahman, Noorsaadah
Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels–Alder adducts morusalbanol A and 441772-64-1
title Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels–Alder adducts morusalbanol A and 441772-64-1
title_full Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels–Alder adducts morusalbanol A and 441772-64-1
title_fullStr Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels–Alder adducts morusalbanol A and 441772-64-1
title_full_unstemmed Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels–Alder adducts morusalbanol A and 441772-64-1
title_short Model studies on construction of the oxabicyclic [3.3.1] core of the mulberry Diels–Alder adducts morusalbanol A and 441772-64-1
title_sort model studies on construction of the oxabicyclic 3 3 1 core of the mulberry diels alder adducts morusalbanol a and 441772 64 1
topic QD Chemistry
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