41299-70-1Relevant academic research and scientific papers
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 J.C.,Lee, Vannajan Sanghiran,Chong, Wei Lim,Khaledi, Hamid,Rahman, Noorsaadah Abd
, p. 5082 - 5085 (2015)
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.
