MyJournals Home  

RSS FeedsTotal synthesis of decarboxyaltenusin (Beilstein Journal of Organic Chemistry)

 
 

22 january 2021 10:17:23

 
Total synthesis of decarboxyaltenusin (Beilstein Journal of Organic Chemistry)
 


Abstract The total synthesis of decarboxyaltenusin (5’-methoxy-6-methyl-[1,1’-biphenyl]-3,3’,4-triol), a toxin produced by various mold fungi, has been achieved in seven steps in a yield of 31% starting from 4-methylcatechol and 1-bromo-3,5-dimethoxybenzene, where the longest linear sequence consists of five steps. The key reaction was a palladium-catalyzed Suzuki coupling of an aromatic boronate with a brominated resorcin derivative. Beilstein J. Org. Chem. 2021, 17, 224–228. doi:10.3762/bjoc.17.22


 
60 viewsCategory: Chemistry
 
[ASAP] Structural and Functional Characterization of Allatostatin Receptor Type-C of Thaumetopoea pityocampa, a Potential Target for Next-Generation Pest Control Agents (Journal of Chemical Information and Modeling)
[ASAP] CFD–PBM Simulation of Liquid–Liquid Dispersions in a Pump-Mixer (Industrial & Engineering Chemistry Research)
 
 
blog comments powered by Disqus


MyJournals.org
The latest issues of all your favorite science journals on one page

Username:
Password:

Register | Retrieve

Search:

Chemistry


Copyright © 2008 - 2021 Indigonet Services B.V.. Contact: Tim Hulsen. Read here our privacy notice.
Other websites of Indigonet Services B.V.: Nieuws Vacatures News Tweets Nachrichten