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- W2058559329 abstract "Abstract A convergent approach to functionalise aromatic compounds with a linker terminated by a phosphonate group is reported. The starting point of this strategy is the synthesis of five new ω‐alkyne‐phosphonates. The linker between the phosphonate group and the alkyne part is either an alkyl or an ether chain. This strategy is based on the use of the phosphonate group as the anchoring point for the attachment of organic compounds onto alumina and the alkyne group, which is used to functionalise aryl halide compounds by a Sonogashira cross‐coupling. The use of 1,10‐phenanthroline as substrate illustrates the application of this strategy to an aromatic ligand. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)" @default.
- W2058559329 created "2016-06-24" @default.
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- W2058559329 date "2007-02-16" @default.
- W2058559329 modified "2023-10-03" @default.
- W2058559329 title "ω‐Alkyne‐Mono‐ and Diphosphonates – Synthesis and Sonogashira Cross‐Coupling Reaction with Aryl Halides" @default.
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- W2058559329 doi "https://doi.org/10.1002/ejoc.200600556" @default.
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