Thioamidoalkylation of 1,3-dicarbonyl compounds, enol silyl ethers, and enamines

被引：1
|
作者：
Katritzky, Alan R. [1 ]
Celik, Ilhami
Abdel-Fattah, Ashraf A. A.
机构：
[1] Univ Florida, Dept Chem, Ctr Heterocycl Gpds, Gainesville, FL 32611 USA
[2] Anadolu Univ, Fac Sci, Dept Chem, TR-26470 Eskisehir, Turkey
[3] Benha Univ, Fac Sci, Dept Chem, Banha, Egypt
来源：
SYNTHESIS-STUTTGART | 2007年 / 11期
关键词：
thioamides; N-(alpha-thioamidoalkyl)benzotriazoles; thioamidoalkylation; 1,3-dicarbonyl compounds; enol silyl ethers; enamines;
D O I：
10.1055/s-2007-966064
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Novel syntheses of beta-thioamido ketones via thioamidoalkylations of malonates, beta-keto esters, beta-diketones, enol silyl ethers, and enamines with N-(alpha-thioamidoalkyl)benzotriazoles are described.
引用
收藏
页码：1655 / 1662
页数：8
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