The Synthesis of α-Azidoesters and Geminal Triazides

被引:83
作者
Klahn, Philipp [1 ]
Erhardt, Hellmuth [1 ]
Kotthaus, Andreas [1 ]
Kirsch, Stefan F. [1 ]
机构
[1] Berg Univ Wuppertal, D-42119 Wuppertal, Germany
关键词
azides; energy-rich compounds; hypervalent iodine compounds; nitrogen; oxidation; BETA-KETO-ESTERS; CRYSTAL-STRUCTURE; CLICK CHEMISTRY; AZIDE REAGENT; GERMANIUM(II) AZIDES; TRIMETHYLSILYL AZIDE; NMR-SPECTROSCOPY; ORGANIC AZIDES; SODIUM-AZIDE; ENOL ETHERS;
D O I
10.1002/anie.201402433
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Three simple methods for the synthesis of geminal triazides are described: Starting from 1) 3-oxocarboxylic acids, 2) iodomethyl ketones, or 3) terminal olefins, a range of triazidomethyl ketones can be constructed under mild oxidative reaction conditions by the use of IBX-SO3K, a sulfonylated derivative of 2-iodoxybenzoic acid (IBX), and NaN3 as an azide source. This is the first report of representatives of this novel class of triazide compounds: Despite their high nitrogen content, the geminal triazides are easy to handle, even when preparative-scale syntheses are performed. (Caution: These procedures still require protective measures!) The triazides are now broadly available for further studies regarding their properties and reactivity. Furthermore, we show how the method can be used to provide alpha-azidoesters, which are potential building blocks for amino acids.
引用
收藏
页码:7913 / 7917
页数:5
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