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...
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: |
Similar Items
-
Mulberry Diels–Alder-type adducts: isolation, structure, bioactivity, and synthesis
by: Si-Yuan Luo, et al.
Published: (2022-09-01) -
Diels-Alder reactions of organotin acetylides and the chemistry of the adducts
by: Evnin, Anthony Basil
Published: (2017) -
Biocatalytic approaches to hetero-Diels-Alder adducts of carbonyl compounds.
by: Gouverneur, V, et al.
Published: (2005) -
Diels–Alder Adducts of Morphinan-6,8-Dienes and Their Transformations
by: János Marton, et al.
Published: (2022-04-01) -
Synthesis of the Formal Diels-Alder Adducts of N-substituted Dehydromaleimides and Anthracene
by: Wim Dehaen, et al.
Published: (2000-02-01)