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- W2016830010 abstract "Enone phosphonates 1 and 2 were found to be excellent dienophiles for the Diels-Alder reaction, giving phosphonate-containing polycycles, and the phosphonate group of the resulting adducts facilitated both the installation of an angular alkyl group via a reductive alkylation process and the regioselective generation of a ring junction double bond via an intramolecular Wadsworth-Horner-Emmons reaction." @default.
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- W2016830010 date "2002-01-17" @default.
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- W2016830010 title "Diels–Alder chemistry of 2-diethoxyphosphinylcyclohex-2-enones. A new approach to complex phosphonates and synthetic applications of the β-keto phosphonate system" @default.
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- W2016830010 doi "https://doi.org/10.1039/b109780f" @default.
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