End-on nitrogen insertion of a diazo compound into a germanium (II) hydrogen bond and a comparable reaction with diethyl azodicarboxylate

Jana, Anukul ; Sen, Sakya S. ; Roesky, Herbert W. ; Schulzke, Carola ; Dutta, Sudipta ; Pati, Swapan K. (2009) End-on nitrogen insertion of a diazo compound into a germanium (II) hydrogen bond and a comparable reaction with diethyl azodicarboxylate Angewandte Chemie International Edition, 48 (23). pp. 4246-4248. ISSN 1433-7851

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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/anie.20...

Related URL: http://dx.doi.org/10.1002/anie.200900617

Abstract

A happy ending: The germanium(II) hydride [LGeH], where L=[HC{(CMe)(2,6-iPr2C6H3N)}2], reacts with a diazoalkane to form the hydrazone derivative (see picture). The reaction proceeds through the unprecedented end-on nitrogen insertion of the diazo compound.

Item Type:Article
Source:Copyright of this article belongs to John Wiley and Sons.
Keywords:Ab Initio Calculations; Diazo Compounds; Insertions; Germanium
ID Code:60842
Deposited On:12 Sep 2011 07:23
Last Modified:12 Sep 2011 07:23

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