84967-87-3Relevant academic research and scientific papers
PHOTODECARBOXYLATIVE CHLORINATION OF CARBOXYLIC ACIDS VIA THEIR BENZOPHENONE OXIME ESTERS
Hasebe, Masato,Tsuchiya, Takashi
, p. 6287 - 6290 (2007/10/02)
Decarboxylative chlorination of various aromatic and aliphatic carboxylic acids is performed successfully by the photolysis of their benzophenone oxime esters in carbon tetrachloride and corresponding chloro compounds are prepared in good yields.High selective generation of the certain radical and efficiency of the stable radical precursor, benzophenone oxime ester, afford much advantage for radical chemistry.
Three Component Reactions. XIV. 2-Imidazolines and 1,2,4-Triazoles by Ring Closure Reactions of N-(2-Chloro-alkyl)imidchlorides with Hydrazine and Hydrazones
Neumann, R.,Beger, J.
, p. 1026 - 1032 (2007/10/02)
N-(2-Chloro-alkyl)benzimidchlorides (1a and 1b) give with hydrazine in dependence on the reaction medium 1,1'-bis(2-imidazolines) (4), 1-benzamido-2-imidazolines (5) or 1,2,4-triazoles (6 and 7) and also N-(2-chloro-alkyl)benzamides (8).From imidchlorides
