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Hydroformylation of Internal Alkenes by Encapsulated Rhodium

Joost N. H. Reek, M. Kuil, Theresa Soltner, Piet van Leeuwen

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Abstract

Significance This is an outstanding report with unprecedented regioselectivity for hydroformylation of internal alkenes. The use of encapsulated rhodium gives extremely high regioselectivity, whereas a standard rhodium catalyst (not encapsulated) gives nearly a 1:1 mixture of isomers. When the reaction is performed at 25 °C, the highest regio­selectivity is obtained, and the selectivity decreases with an increase in temperature due to isomerization pathways capable at the elevated temperatures.

About this research paper

What this paper is about

Significance This is an outstanding report with unprecedented regioselectivity for hydroformylation of internal alkenes. The use of encapsulated rhodium gives extremely high regioselectivity, whereas a standard rhodium catalyst (not encapsulated) gives nearly a 1:1 mixture of isomers. When the reaction is performed at 25 °C, the highest regio­selectivity is obtained, and the selectivity decreases with an increase in temperature due to isomerization pathways capable at the elevated temperatures.

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Available abstract

Significance This is an outstanding report with unprecedented regioselectivity for hydroformylation of internal alkenes. The use of encapsulated rhodium gives extremely high regioselectivity, whereas a standard rhodium catalyst (not encapsulated) gives nearly a 1:1 mixture of isomers. When the reaction is performed at 25 °C, the highest regio­selectivity is obtained, and the selectivity decreases with an increase in temperature due to isomerization pathways capable at the elevated temperatures.

Key concepts: Hydroformylation, Regioselectivity, Rhodium, Chemistry, Isomerization, Selectivity, Catalysis, Organic chemistry

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