1994
DOI: 10.1006/jcat.1994.1120
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Rhodium-Catalyzed Aldol-Type Chemistry Under Syngas: Selective Reductive Dimerizations of Aldehydes to Monoaldehydes and Further Oxidation to nor-Ketones

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“…Dimerization with the use of 111a and b in combination with additives (PPh 3 , PPh 3 + H 2 O, or H 2 O), which proved to be the catalytic systems of choice in this reaction, gave products in moderate to good yields (up to 90%). However, the selectivity of the formation of all these homocoupling compounds remained poor as compared to that observed with Wilkinson's catalyst, which afforded DFBAL in 80% yield along with insignificant amounts (<2%) of two other coupling products, DFBOL and DFBEAL [104].…”
Section: Metallacarboranes With η 3 η 2 -Cycloallylolefinic-type Ligcontrasting
confidence: 48%
“…Dimerization with the use of 111a and b in combination with additives (PPh 3 , PPh 3 + H 2 O, or H 2 O), which proved to be the catalytic systems of choice in this reaction, gave products in moderate to good yields (up to 90%). However, the selectivity of the formation of all these homocoupling compounds remained poor as compared to that observed with Wilkinson's catalyst, which afforded DFBAL in 80% yield along with insignificant amounts (<2%) of two other coupling products, DFBOL and DFBEAL [104].…”
Section: Metallacarboranes With η 3 η 2 -Cycloallylolefinic-type Ligcontrasting
confidence: 48%