Base-catalysed oxidative [3+2]cycloaddition reaction of [60]fullerene with beta-dicarbonyl compounds

被引:32
作者
Ohno, M [1 ]
Yashiro, A [1 ]
Eguchi, S [1 ]
机构
[1] NAGOYA UNIV, FAC ENGN, INST APPL ORGAN CHEM, CHIKUSA KU, NAGOYA, AICHI 46401, JAPAN
关键词
D O I
10.1039/cc9960000291
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The ambiphilic nature of beta-keto esters and beta-diketones allows cycloaddition to C-60 in the presence of piperidine to give dihydrofuran-fused C-60 derivatives via oxidative cyclization complimentary to the concerted process.
引用
收藏
页码:291 / 292
页数:2
相关论文
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VINOGRADOV MG, 1988, SYNTHESIS-STUTTGART, P60
[32]   1,3-DIPOLAR CYCLOADDITION OF N-BENZYL AZOMETHINE YLIDE TO C-60 - FORMATION OF A C-60-FUSED N-BENZYLPYRROLIDINE [J].
ZHANG, XJ ;
WILLEMS, M ;
FOOTE, CS .
TETRAHEDRON LETTERS, 1993, 34 (51) :8187-8188