Iridium-Catalyzed Hydrogen Transfer Reactions
Saidi, O. and Williams, J. M. J., 2011. Iridium-Catalyzed Hydrogen Transfer Reactions. In: Iridium Catalysis. Berlin: Springer, pp. 77-106. (Topics in Organometallic Chemistry)
Related documents:This repository does not currently have the full-text of this item.
You may be able to access a copy if URLs are provided below.
This chapter describes the application of iridium complexes to catalytic hydrogen transfer reactions. Transfer hydrogenation reactions provide an alternative to direct hydrogenation for the reduction of a range of substrates. A hydrogen donor, typically an alcohol or formic acid, can be used as the source of hydrogen for the reduction of carbonyl compounds, imines, and alkenes. Heteroaromatic compounds and even carbon dioxide have also been reduced by transfer hydrogenation reactions. In the reverse process, the oxidation of alcohols to carbonyl compounds can be achieved by iridium-catalyzed hydrogen transfer reactions, where a ketone or alkene is used as a suitable hydrogen acceptor. The reversible nature of many hydrogen transfer processes has been exploited for the racemization of alcohols, where temporary removal of hydrogen generates an achiral ketone intermediate. In addition, there is a growing body of work where temporary removal of hydrogen provides an opportunity for using alcohols as alkylating agents. In this chemistry, an iridium catalyst "borrows" hydrogen from an alcohol to give an aldehyde or ketone intermediate, which can be transformed into either an imine or alkene under the reaction conditions. Return of the hydrogen from the catalyst provides methodology for the formation of amines or C-C bonds where the only by-product is typically water.
|Item Type||Book Sections|
|Creators||Saidi, O.and Williams, J. M. J.|
|Uncontrolled Keywords||transfer hydrogenation,n-alkylation,c-alkylation,asymmetric transfer hydrogenation,oxidation,alkenes,alcohols,reduction,imines,ketones|
|Departments||Faculty of Science > Chemistry|
|Additional Information||Book series: Topics in Organometallic Chemistry. Volume 34.|
Actions (login required)