Unknown

Dataset Information

0

Palladium/Rhodium Cooperative Catalysis for the Production of Aryl Aldehydes and Their Deuterated Analogues Using the Water-Gas Shift Reaction.


ABSTRACT: A novel Pd/Rh dual-metallic cooperative catalytic process has been developed to effect the reductive carbonylation of aryl halides in moderate to good yield. In this reaction, water is the hydride source, and CO serves both as the carbonyl source and the terminal reductant through the water-gas shift reaction. The catalytic generation of the Rh hydride allows for the selective formation of highly hindered aryl aldehydes that are inaccessible through previously reported reductive carbonylation protocols. Moreover, aldehydes with deuterated formyl groups can be efficiently and selectively synthesized using D2 O as a cost-effective deuterium source without the need for presynthesizing the aldehyde.

SUBMITTER: Ibrahim MYS 

PROVIDER: S-EPMC6173325 | biostudies-literature | 2018 Aug

REPOSITORIES: biostudies-literature

altmetric image

Publications

Palladium/Rhodium Cooperative Catalysis for the Production of Aryl Aldehydes and Their Deuterated Analogues Using the Water-Gas Shift Reaction.

Ibrahim Malek Y S MYS   Denmark Scott E SE  

Angewandte Chemie (International ed. in English) 20180717 32


A novel Pd/Rh dual-metallic cooperative catalytic process has been developed to effect the reductive carbonylation of aryl halides in moderate to good yield. In this reaction, water is the hydride source, and CO serves both as the carbonyl source and the terminal reductant through the water-gas shift reaction. The catalytic generation of the Rh hydride allows for the selective formation of highly hindered aryl aldehydes that are inaccessible through previously reported reductive carbonylation pr  ...[more]

Similar Datasets

| S-EPMC6685968 | biostudies-literature
| S-EPMC6430613 | biostudies-literature
| S-EPMC6879102 | biostudies-literature
| S-EPMC8008838 | biostudies-literature
| S-EPMC4212655 | biostudies-literature
| S-EPMC3235049 | biostudies-literature
| S-EPMC5396316 | biostudies-literature
| S-EPMC8662739 | biostudies-literature
| S-EPMC7075342 | biostudies-literature
| S-EPMC6814718 | biostudies-literature