Publications by authors named "Akihiko Iwashita"

α-Quaternary ketones are accessed through novel enantioselective alkylations of allyl and propargyl electrophiles by unstabilized prochiral enolate nucleophiles in the presence of palladium complexes with various phosphinooxazoline (PHOX) ligands. Excellent yields and high enantiomeric excesses are obtained from three classes of enolate precursor: enol carbonates, enol silanes, and racemic β-ketoesters. Each of these substrate classes functions with nearly identical efficiency in terms of yield and enantioselectivity.

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The synthesis of a new class of fullerene derivatives, 1-imino-4-silylmethyl[60]fullerene derivatives, is described. The anion (C(60)R(1-)) of an alkyl- or aryl-adduct of [60]fullerene, C(60)R(1)H (R(1) = CH(2)SiMe(3), CH(2)SiMe(2)Ph, C(6)H(4)-OMe-4, C(6)H(4)-NMe(2)-4, C(6)H(4)-CF(3)-4 and C(6)H(4)-OMe-2), was allowed to react with a nitrilium salt [R(2)CNCH(2)SiMe(3)][OTf] (Tf = SO(2)CF(3)) that was generated in situ by the reaction of Me(3)SiCH(2)OTf and a nitrile solvent R(1)CN (R(2) = Ph and Me). The desired imino[60]fullerene derivative C(60)(R(1)) [C(=NCH(2)SiMe(3))R(2)] was produced in a yield up to 80%.

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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, C60R(1)H, in good yield (up to 93% isolated yield). The hydrofullerene was then deprotonated to generate the corresponding anion, C60R(-), which was then alkylated to obtain 58pi-electron di(organo)[60]fullerenes, C60R(1)R(2), in good to high yield (up to 93% overall yield). The two-step methodology provides a wide variety of 1,4-di(organo)[60] fullerenes bearing the same or different organic addends on the [60] fullerene core.

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