Literature DB >> 24895221

The synthesis of α-azidoesters and geminal triazides.

Philipp Klahn1, Hellmuth Erhardt, Andreas Kotthaus, Stefan F Kirsch.   

Abstract

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-SO3 K, 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 α-azidoesters, which are potential building blocks for amino acids.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  azides; energy-rich compounds; hypervalent iodine compounds; nitrogen; oxidation

Mesh:

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Year:  2014        PMID: 24895221     DOI: 10.1002/anie.201402433

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Iron-Catalyzed Direct Diazidation for a Broad Range of Olefins.

Authors:  Yong-An Yuan; Deng-Fu Lu; Yun-Rong Chen; Hao Xu
Journal:  Angew Chem Int Ed Engl       Date:  2015-11-23       Impact factor: 15.336

2.  A Synthetic Route Toward Tetrazoles: The Thermolysis of Geminal Diazides.

Authors:  Kristina Holzschneider; My Linh Tong; Fabian Mohr; Stefan F Kirsch
Journal:  Chemistry       Date:  2019-08-13       Impact factor: 5.236

  2 in total

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