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Updated: Apr 11, 2026
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Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions
Published on: July 17, 2020
Synthesis of the diaryl ether cores common to chrysophaentins A, E and F
Anthony J Brockway1, Charles I Grove1, Maximillian E Mahoney1
1Department of Chemistry, University of California, One Shields Ave, Davis, CA 95616.
Abstract:
The synthesis of the diaryl ether subunits of the marine natural products chrysophaentin A, E and F is described. These natural prodcuts feature tetrasubstituted benzene rings with complex substitution patterns. The central strategy involves an SNAr reaction between a complex phenol and a polysubstituted fluoronitrobenzene. Subseqent attempts to construct the unusual E-chloroalkene linkage through several different approaches are also disclosed.
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