137250-77-2Relevant academic research and scientific papers
Anionic [3, 3] rearrangements of cyclic hydrazine diacylates to medium-size cyclic diamides and their structures
Endo, Yasuyuki,Uchida, Takuya,Yamaguchi, Kentaro
, p. 151 - 158 (2007/10/03)
The anionic rearrangement of N, N′-dimethyl-N, N′-diacylhydrazines to 1, 2-disubstituted succinamides proceeds in the presence of a ajacent enolatestabilizing substituent such as a phenyl group. However, a substituent that poorly stabilizes the cc-carbani
Anionic 3,4-diaza[3,3]sigmatropic rearrangements of N,N′-diacylhydrazines
Endo, Yasuyuki,Shudo, Koichi
, p. 4517 - 4520 (2007/10/02)
N,N′-Diacylhydrazines rearrange under basic conditions to afford 1,2-disubstituted succinamides. The rearrangement can be rationalized in terms of [3,3]sigmatropic shifts of biscarboxamide enolates.
