156551-17-6Relevant articles and documents
Silylmethylations of C60 with Grignard Reagents: Selective Synthesis of HC60CH2SiMe2Y and C60(CH2SiMe2Y)2 with Selection of Solvents
Nagashima, Hideo,Terasaki, Hiroshi,Kimura, Eiji,Nakajima, Katsumasa,Itoh, Kenji
, p. 1246 - 1248 (1994)
Addition reactions of Me2SiYCH2MgCl (1) to C60 provided two products, HC60CH2SiYMe2 (2) and 2C60 (3) (Y = Me, H, CH=CH2, Ph, O-iPr).Selective preparation of either 2 or 3 was accomplished by selection of the solvent; 2 was formed in THF, wherea
Regioselective synthesis of 1,4-di(organo)[60]fullerenes through DMF-assisted monoaddition of silylmethyl Grignard reagents and subsequent alkylation reaction
Matsuo, Yutaka,Iwashita, Akihiko,Abe, Yoko,Li, Chang-Zhi,Matsuo, Keiko,Hashiguchi, Masahiko,Nakamura, Eiichi
supporting information; experimental part, p. 15429 - 15436 (2009/03/11)
Monoaddition of Grignard reagents, in particular tri(organo) silylmethylmagnesium chlorides, to [60]fullerene took place smoothly in the presence of dimethylformamide to produce (organo)(hydro)[60]fullerenes, C 60C)R1H, in good yield