52056-24-3Relevant articles and documents
Rhodium-catalyzed addition of arylstannanes to carbon-heteroatom double bond
Oi, Shuichi,Moro, Mitsutoshi,Fukuhara, Hiroe,Kawanishi, Takanori,Inoue, Yoshio
, p. 4351 - 4361 (2007/10/03)
The addition of arylstannanes to the carbon-heteroatom double bond in the presence of a catalytic amount of a cationic rhodium complex ([Rh(cod)(MeCN)2]BF4) was examined. The reactions of aldehydes, α-dicarbonyl compounds, and N-substituted aldimines with the arylstannanes gave corresponding alcohols, α-hydroxy carbonyl compounds, and amines, respectively. An arylrhodium complex generated by the transmetalation with the arylstannane was probably the active catalytic species.
Regioselective superacid-catalyzed electrocyclization of diphenylmethyl cations to fluorenes, phenanthrols and benzofurans
Yoshida,Ohwada
, p. 1487 - 1494 (2007/10/03)
Cationic electrocyclization of α-benzoyldiphenylmethanols in the presence of superacid provides fluorenes, phenanthrols and benzofurans in good to moderate yields. A single substitution leads to regioselective cationic electrocyclizations.
Samarium(II) iodide promoted novel reductive coupling reactions of ketones and nitriles
Zhou, Longhu,Zhang, Yongmin,Shi, Daqing
, p. 8491 - 8494 (2007/10/03)
The intramolecular and intermolecular reductive coupling reaction of ketones-nitriles promoted by SmI2 were studied.
