Phosphine-Catalyzed Domino Regio- and Stereo-Selective Hexamerization of 2-(Bromomethyl)acrylates to 1,2-Bis(cyclohexenyl)ethenyl Derivatives
Articolo
Data di Pubblicazione:
2023
Citazione:
Phosphine-Catalyzed Domino Regio- and Stereo-Selective Hexamerization of 2-(Bromomethyl)acrylates to 1,2-Bis(cyclohexenyl)ethenyl Derivatives / M. Papis, R. Bucci, A. Contini, M.L. Gelmi, L. Lo Presti, G. Poli, G. Broggini, C. Loro. - 25:40(2023 Oct 13), pp. 7380-7384. [10.1021/acs.orglett.3c02836]
Abstract:
A phosphine-catalyzed domino assembly of six units of 2-bromomethyl acrylates afforded polyalkenyl adducts containing two cyclohexenyl rings. This reaction occurs under mild conditions providing the final product by formation of seven carbon-carbon bonds and four stereocenters. Experimental and computational studies support an initial dimerization of the substrate, which in turn trimerizes involving two totally regio- and stereocontrolled Diels-Alder cycloadditions. The yield of the hexamerization of the 2-bromomethyl acrylates depends on the size of the ester function. The protocol has also proved to be practicable on a gram scale.
Tipologia IRIS:
01 - Articolo su periodico
Elenco autori:
M. Papis, R. Bucci, A. Contini, M.L. Gelmi, L. Lo Presti, G. Poli, G. Broggini, C. Loro
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