74804-41-4Relevant academic research and scientific papers
REGIOSELECTIVE CYCLOADDITIONS OF 1H-AZEPINE AND 1H-1,2-DIAZEPINE DERIVATIVES WITH N,α-DIPHENYLNITRONE AND NITROSOBENZENE
Saito, Katsuhiro,Yoshino, Akihiro,Watanabe, Hiroyuki,Takahashi, Kensuke
, p. 497 - 504 (2007/10/02)
Reactions of 1-carbomethoxy-1H-azepine with N,α-diphenylnitrone afforded endo- and exo--type cycloadducts in almost the same ratio.Reactions of 1-carboethoxy-1H-azepine with nitrosobenzene in chloroform afforded - and -types of cycloadducts.Analogous results were obtained in the reactions using 1-carboethoxy-1H-1,2-diazepine.
1,4-CYCLOADDITION OF NITROSOBENZENE TO N-ETHOXYCARBONYLAZEPINE
Murphy, William S.,Raman, Krishna P.
, p. 319 - 320 (2007/10/02)
A new stable product from the reaction of nitrosobenzene and N-ethoxycarbonylazepine is shown to be a 1,4-cycloadduct.
