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Synthesis 2016; 48(04): 557-565
DOI: 10.1055/s-0035-1560912
DOI: 10.1055/s-0035-1560912
paper
Parameters Influencing Reactivity and Regioselectivity in the Methoxycarbonylation of Arylalkenes
Weitere Informationen
Publikationsverlauf
Received: 15. September 2015
Accepted after revision: 12. Oktober 2015
Publikationsdatum:
25. November 2015 (online)
Abstract
Previous research showed that the steric bulk, electronic character, and bite angle of the ligand have an influence on both the catalyst activity and regioselectivity of hydroformylation and hydroesterification reactions. However, little is known in this regard about the influence of the steric and electronic environment around the double bond of the substrate. A variety of arylalkenes were therefore subjected to methoxycarbonylation to investigate the steric and electronic effects of substituents on the aromatic ring of the substrate on the regioselectivity and reactivity in the methoxycarbonylation reaction of these substrates with a Pd(II)/Al(OTf)3/Ph3P catalyst system.
Supporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0035-1560912.
- Supporting Information
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