New trifluoromethyl-substituted heterocycles by multicomponent reactions of siloxycyclopropanes

被引:4
|
作者
Gladow, Daniel [1 ]
Senf, Deborah [1 ]
Wiecko, Jelena [1 ]
Lentz, Dieter [1 ]
Zimmer, Reinhold [1 ]
Reissig, Hans-Ulrich [1 ]
机构
[1] Free Univ Berlin, Inst Chem & Biochem, 3 Takustr, D-14195 Berlin, Germany
关键词
amino acids; cyclopropanes; isonitriles; gamma-lactams; pyridines; multicomponent reactions; DONOR-ACCEPTOR CYCLOPROPANES; 4-COMPONENT REACTION; AMINO-ACIDS; 3-COMPONENT CONDENSATION; ORGANIC-SYNTHESIS; UGI; 5-CENTER; DERIVATIVES; CHEMISTRY; ISOCYANIDES; ALDEHYDES;
D O I
10.1007/s10593-017-2068-y
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Multicomponent reactions of ethyl 1-trifluoromethyl-2-(trimethylsilyloxy)cyclopropanecarboxylate, isonitriles, and either 2-aminopyridine or amino acids provided imidazo[1,2-a]pyridines or gamma-lactams, respectively. This access to trifluoromethyl-substituted heterocycles demonstrates again that siloxycyclopropanes can serve as hidden functionalized aldehydes and that this type of donor-acceptor-substituted cyclopropanes is particularly versatile.
引用
收藏
页码:416 / 421
页数:6
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