Organoaluminum hydrides catalyzed hydroboration of carbonates, esters, carboxylic acids, and carbon dioxide

Ben Yan, Sayan Dutta, Xiaoli Ma*, Congjian Ni, Debasis Koley*, Zhi Yang*, Herbert W. Roesky*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

27 Citations (Scopus)

Abstract

The reductive functionalization of the C O unit of carbonates, carboxylic acids, esters, and CO2, respectively has received great attention since its introduction. This method is often used industrially for the synthesis of high value-added energy products in chemistry. This opens up a new way forward to reduce greenhouse gases and the consumption of traditional energy sources. Herein, we report an earth-abundant, cheap, and readily available aluminum dihydride, which can catalyze the reduction of a range of carbonates, esters, carboxylic acids, and CO2, respectively in the presence of pinacolborane as a reducing agent. Moreover, we demonstrate that the reaction can proceed to obtain good yield products under mild conditions, with low catalyst loading and solvent-free reactions. The mechanism of the catalytic reduction of carbonates has been investigated.

Original languageEnglish
Pages (from-to)6756-6765
Number of pages10
JournalDalton Transactions
Volume51
Issue number17
DOIs
Publication statusPublished - 8 Apr 2022

Fingerprint

Dive into the research topics of 'Organoaluminum hydrides catalyzed hydroboration of carbonates, esters, carboxylic acids, and carbon dioxide'. Together they form a unique fingerprint.

Cite this