90712-52-0Relevant academic research and scientific papers
4,5-dihydroisoxazoles from arylcyclopropanes: II. Reaction of arylcyclopropanes with nitrosyl chloride activated by sulfur(VI) oxide
Bondarenko,Gavrilova,Kazantseva,Tikhanushkina,Nifant'ev,Saginova,Zyk
, p. 564 - 570 (2008/02/02)
Arylcyclopropanes react with nitrosyl chloride activated by sulfur(VI) oxide to give the corresponding 5-aryl-4,5-dihydro-1,2-oxazoles in quantitative yields. The complex NOC1?2SO3 is a highly efficient nitrosating agent which makes it possible to involve in the process arylcyclopropanes having both donor and acceptor substituents in the aromatic ring. Nauka/Interperiodica 2007.
2-Isoxazolines from arylcyclopropanes: I. Monoarylcyclopropanes in a reaction with nitrosyl chloride activated by sulfur(IV) oxide
Bondarenko,Gavrilova,Kazantseva,Tikhanushkina,Nifant'ev,Saginova,Zyk
, p. 249 - 255 (2007/10/03)
A reaction of monoarylcyclopropanes with nitrosyl chloride activated by sulfur (IV) oxide gave in good yields 5-arylisoxazolines. The reaction is of electrophilic character. A scheme of the reaction was suggested. Pleiades Publishing, Inc. 2006.
SUBSTITUTED PHENYLCYCLOPROPANES IN THE SYNTHESIS OF 2-ISOXAZOLINES
Gazzaeva, R. A.,Shabarov, Yu. S.,Saginova, L. G.
, p. 246 - 250 (2007/10/02)
Diverse 2-isoxazolines with substituents in both the aromatic ring and isoxazoline ring were obtained in the process of nitrosation of various substituted phenylcyclopropanes with sodium nitrite in mixture of chloroform and trifluoroacetic acid.
