Issue 41, 2024

Synthesis of unsymmetrical 2,4-diaryl substituted and 3-bromo-2-(4-bromoalkoxy)-derived pyranocoumarins

Abstract

A series of unsymmetrical 2,4-disubstituted pyranocoumarins and 3-bromo-2-(4-bromoalkoxy)-derived pyranocoumarins were synthesized via the palladium-catalyzed C–H arylation of 4-phenyl-4H,5H-pyrano[3,2-c]chromen-5-ones with aryl iodide and the three-component reaction of 4-phenyl-4H,5H-pyrano[3,2-c]chromen-5-one with bromine and cyclic ether, respectively.

Graphical abstract: Synthesis of unsymmetrical 2,4-diaryl substituted and 3-bromo-2-(4-bromoalkoxy)-derived pyranocoumarins

Supplementary files

Article information

Article type
Paper
Submitted
16 Aug 2024
Accepted
11 Sep 2024
First published
16 Sep 2024

Org. Biomol. Chem., 2024,22, 8310-8316

Synthesis of unsymmetrical 2,4-diaryl substituted and 3-bromo-2-(4-bromoalkoxy)-derived pyranocoumarins

V. Saravanan, P. Lin and D. Yang, Org. Biomol. Chem., 2024, 22, 8310 DOI: 10.1039/D4OB01353K

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