Nair, Vijay ; Biju, A. ; Mathew, Smitha (2007) The Reaction of Huisgen Zwitterion with Diaryl-1,2-diones and Ketones: An Efficient Protocol for Carbon-Nitrogen Bond Formation Synthesis, 2007 (5). pp. 697-704. ISSN 0039-7881
Full text not available from this repository.
Official URL: http://doi.org/10.1055/s-2007-965910
Related URL: http://dx.doi.org/10.1055/s-2007-965910
Abstract
The reaction of Huisgen zwitterion, derived from triphenylphosphine and dialkyl azodicarboxylate, with diaryl-1,2-diones afforded N,N-dicarboalkoxy monohydrazones via a mechanistically novel rearrangement. Cyclic and acyclic ketones furnished vinyl hydrazinedicarboxylates under similar conditions.
Item Type: | Article |
---|---|
Source: | Copyright of this article belongs to Georg Thieme Verlag KG |
ID Code: | 128747 |
Deposited On: | 03 Nov 2022 06:57 |
Last Modified: | 03 Nov 2022 06:57 |
Repository Staff Only: item control page