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Synthesis 2016; 48(23): 4155-4160
DOI: 10.1055/s-0035-1562456
DOI: 10.1055/s-0035-1562456
paper
Palladium-Catalyzed Asymmetric 1,6-Addition of Diarylphosphines to Allylidenemalonates for Chiral Phosphine Synthesis
Further Information
Publication History
Received: 14 April 2016
Accepted after revision: 02 June 2016
Publication Date:
10 August 2016 (online)
Abstract
A pincer-palladium-catalyzed asymmetric 1,6-addition of diarylphosphines to allylidenemalonates has been developed for the synthesis of chiral allylic phosphines with up to 89% ee under mild conditions.
Key words
asymmetric 1,6-addition - pincer palladium catalyst - chiral phosphines - allylidenemalonatesSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0035-1562456.
- Supporting Information
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For reviews on catalytic asymmetric synthesis of chiral phosphines, see:
For leading examples, see:
For catalytic asymmetric 1,4-addition of substituted phosphines or phosphine oxides to electron-deficient alkenes, see:
For reviews on asymmetric 1,4-addition reactions, see:
For reviews on asymmetric 1,6-addition reactions, see:
For rhodium/iridium-catalyzed 1,6-addition reactions, see:
For copper-catalyzed asymmetric 1,6-addition reactions, see:
For organocatalyzed asymmetric 1,6-addition reactions, see:
For reviews on pincer metal complexes, see:
For synthesis and application of chiral PCP–PdCl complexes, see: