122491-18-3Relevant academic research and scientific papers
In(+3) as a chemoselectivity switch for TMM-PDL2 cycloadditions to ynones
Trost, Barry M.,Sharma, Sunaina,Schmidt, Thomas
, p. 7183 - 7186 (1993)
The previous inability to effect palladium catalyzed cycloadditions of 2-trimethylsilylmethallyl acetate to the carbonyl group of ynones is rectified by the employment of indium acetylacetonoate as a co-catalyst.
Palladium-Catalyzed Trimethylenemethane Reaction To Form Methylenetetrahydrofurans. Aldehyde and Ketone Substrates and the Tin Effect
Trost, Barry M.,King, Steven A.,Schmidt, Thomas
, p. 5902 - 5915 (2007/10/02)
The palladium-catalyzed trimethylenemethane (TMM) cycloaddition of carbonyl compounds has been shown to have a strong dependence upon the presence of cocatalysts such as tri-n-butyltin acetate, di-n-butyltin diacetate, or trimethyltin acetate.High-yieldin
