Reaction of diaryl-1,2-diones with triphenylphosphine and diethyl azodicarboxylate leading to N,N-dicarboethoxy monohydrazones via a novel rearrangement

dc.contributor.author	Vijay Nair, G
dc.contributor.author	Biju, A T
dc.contributor.author	Abhilash, K G
dc.contributor.author	Rajeev S Menon
dc.contributor.author	Suresh, E
dc.date.accessioned	2021-02-08T11:59:12Z
dc.date.available	2021-02-08T11:59:12Z
dc.date.issued	2005
dc.identifier.citation	Organic Letters 7(11):2121-2123; 26 May 2005	en_US
dc.identifier.issn	1523-7060
dc.identifier.uri	http://hdl.handle.net/123456789/3662
dc.description.abstract	A mechanistically novel reaction of diaryl-1,2-diones with diethyl azodicarboxylate and triphenylphosphine to afford N,N-dicarboethoxy monohydrazones is described. The reaction proceeds via a nitrogen to nitrogen migration of a carboethoxy group.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Diaryl-1,2-diones	en_US
dc.subject	Triphenylphosphine	en_US
dc.subject	Diethyl azodicarboxylate	en_US
dc.subject	N,N-dicarboethoxy monohydrazones	en_US
dc.title	Reaction of diaryl-1,2-diones with triphenylphosphine and diethyl azodicarboxylate leading to N,N-dicarboethoxy monohydrazones via a novel rearrangement	en_US
dc.type	Article	en_US