A Morita–Baylis–Hillman adduct allows the diastereoselective synthesis of styryl lactones
Author:
Funder
Fapesp
CNPq
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference76 articles.
1. Styryl-lactones from Goniothalamus species— A review
2. Cytotoxic Activity of Styryl Lactones and their Derivatives
3. Styryl Lactones and Their Derivatives: Biological Activities, Mechanisms of Action and Potential Leads for Drug Design
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3. Divergent Synthesis and Biological Evaluation of 2,6-Disubstituted Tetrahydropyran-Containing Natural Products: Parvistone E, Goniothalesdiol A, 6-epi-Goniothalesdiol A, and 8-epi-9-Deoxygoniopypyrone;Synthesis;2023-08-07
4. First diastereoselective total synthesis of bicyclic styryl lactone: (1R,5R,7R)-7-((E)-styryl)-2,6-dioxabicyclo[3.3.1]nonan-3-one;Results in Chemistry;2023-01
5. Morita Baylis Hillman Adduct Serves as Ligand in the Synthesis of Transition Metal Complexes Exhibiting Antibacterial Activity;Pharmaceutical Chemistry Journal;2022-10
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