134810-87-0Relevant academic research and scientific papers
Anionic hetero[3,3] and [3,5][ rearrangements of hydroxylamine derivatives accompanied with N-O bond cleavage
Endo,Uchida,Hizatate,Shudo
, p. 1096 - 1105 (2007/10/02)
Aromatic and aliphatic N,O-divinylhydroxylamine systems generated in situ from hydroxylamine derivatives smoothly undergo [3,3] rearrangement. The base-catalyzed formation and rearrangement of enolates or dienolates of N-aryl-O-acylhydroxylamines, N,O-dia
Herbicidal N-isopropylheteroaryloxyacetanilides
-
, (2008/06/13)
Herbicidal N-isopropylheteroaryloxyacetanilides of the formula STR1 in which A stands for nitrogen or the group C--R3 where R3 stands for halogen, cyano, alkyl, halogenoalkyl, alkoxy, halogenoalkoxy, alkylthio, halogenoalkylthio, alk
