Sterically Hindered Benzophenones via Rhodium-Catalyzed Oxidative Arylation of Aldehydes
Year: 2008
Type: article
Abstract: Efficient cross-coupling, allowing a straightforward access to congested benzophenones, between aromatic aldehydes and potassium aryltrifluoroborates, is described in the presence of a rhodium/tri-tert-butylphosphane catalyst system and acetone as cosolvent. The use of the stable phosphonium salts of tri-tert-butylphosphane prevented the use of highly oxidizable tri-tert-butylphosphane and allowed a careful control of the stoichiometry with the rhodium.
Source: The Journal of Organic Chemistry
DOI: 10.1021/jo801460w
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: green
OpenAlex ID: W2077523005
