Diels-Alder [4+2]cycloaddition reactions involving C60 and C70 fullerenes

被引:0
作者
García, MM
Klimova, E
García, RAV
Pérez, RG
机构
[1] Univ Nacl Autonoma Mexico, Dept Quim Organ, Inst Quim, Mexico City 04510, DF, Mexico
[2] Univ Autonoma Puebla, Fac Ciencias Quim, Ctr Invest, Puebla, Pue, Mexico
关键词
cycloadditions; Diels-Alder; dienes; quinuclidine; chiral diimines; fullerenes;
D O I
暂无
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
For first time dienes conjugated 8, 9 and 10 were synthesized with a s-cis conformation, and Diels-Alder cycloaddition reactions between dienes synthesized and C-60 and C-70 were carried out, and the results obtained by NMR H-1 and C-13 and elemental analysis demonstrated that the mono and biadduct compounds were formated, diene 9 was more reactive than dienes 8 and 10. Fullerenes C-60 and C-70 did not presented any difference in their reactivity like dienophiles.
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页码:126 / 131
页数:6
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