91361-10-3Relevant academic research and scientific papers
Iron-catalyzed pinacol coupling of aryl ketones with a phenyltitanium reagent: A new type of catalytic reaction
Hayashi, Tamio,Sasaki, Keigo
supporting information; experimental part, p. 492 - 494 (2011/06/25)
A reaction of aryl ketones with phenyltitanium triisopropoxide ([PhTi(Oi-Pr)3]) in the presence of [Fe(acac)3] as a catalyst (1 mol%) gave the corresponding pinacols in high yields. The catalytic cycle of this process involves an iron-catalyzed disproportionation of [PhTi(Oi-Pr) 3] into biphenyl and a lowvalent titanium species.
Efficient method for the preparation of pinacols derived from aromatic and aliphatic ketones by using low-valent titanium reagents in dichloromethane-pivalonitrile
Kagayama,Igarashi,Mukaiyama
, p. 657 - 665 (2007/10/03)
The reductive coupling reaction of aldehydes and ketones, including unsymmetrical aliphatic ketones, proceeded smoothly to give the corresponding pinacols in good to high yields under mild conditions by using combination of titanium(II) chloride and zinc or titanium(IV) chloride and zinc in dichloromethane-pivalonitrile. Meso-selective formation of the coupling products was observed in the cases of some aliphatic ketones. The diastereoselectivities of coupling products depend on both difference of bulkiness of 2-, and 2'-substituents of carbonyl group of the reactant, and overall steric effect around the carbonyl groups.
