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Synthesis 2019; 51(06): 1435-1444
DOI: 10.1055/s-0037-1610332
DOI: 10.1055/s-0037-1610332
paper
Metal-Free Synthesis of Biaryl- and Teraryl-Cored Diarylmethanes by Ring Transformation of 2H-Pyran-2-ones
Weitere Informationen
Publikationsverlauf
Received: 06. September 2018
Accepted after revision: 26. Oktober 2018
Publikationsdatum:
30. November 2018 (online)
Abstract
An efficient metal-free approach for the synthesis of functionalized biaryl-cored diarylmethanes is described by the ring transformation of 2H-pyran-2-ones using 4-phenylbutan-2-one as carbanion source. Moreover, 2H-pyran-2-ones were reacted with 1,3-diphenylacetone in the presence of base to achieve functionalized teraryl-cored diarylmethanes. All the ring transformation reactions were performed under mild reaction conditions to afford the biaryl- and teraryl-cored reaction products in high yields.
Key words
biaryl-cored diarylmethanes - teraryl-cored diarylmethanes - 2H-pyran-2-ones - carbanion - ring transformation reactions - 4-phenylbutan-2-one - 1,3-diphenylacetoneSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0037-1610332.
- Supporting Information
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