Regioselective functionalisation of 2-(diphenylphosphino) pyridine: direct lithiation at the pyridine C-6 position
Identifieur interne : 001B46 ( Main/Exploration ); précédent : 001B45; suivant : 001B47Regioselective functionalisation of 2-(diphenylphosphino) pyridine: direct lithiation at the pyridine C-6 position
Auteurs : Philippe Gros [France] ; Christophe Ben Younès-Millot [France] ; Yves Fort [France]Source :
- Tetrahedron Letters [ 0040-4039 ] ; 2000.
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Abstract
Abstract: It is shown that 2-(diphenylphosphino)pyridine was efficiently and regioselectively metallated at the C-6 position by use of the BuLi–Me2N(CH2)2OLi basic system. The method described opened access to various functionally potential ligands or ligand precursors.
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DOI: 10.1016/S0040-4039(99)02079-1
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Le document en format XML
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<term>Ligand</term>
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<front><div type="abstract" xml:lang="en">Abstract: It is shown that 2-(diphenylphosphino)pyridine was efficiently and regioselectively metallated at the C-6 position by use of the BuLi–Me2N(CH2)2OLi basic system. The method described opened access to various functionally potential ligands or ligand precursors.</div>
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