113327-84-7Relevant academic research and scientific papers
The regioselectivity of nitrone and nitrile oxide cycloadditions to alkylidenecyclopropanes
Brandi, Alberto,Cordero, Franca M.,De Sarlo, Francesco,Gandolfi, Remo,Rastelli, Andrea,Bagatti, Marisa
, p. 3323 - 3334 (1992)
The 1,3-dipolar cycloaddition of nitrile oxides and a nitrone to alkylidencyclopropanes 1-5,used as model for methylenecyclopropanes substituted with aryl group (1), electron-releasing groups (2 and 3) and electron-attracting groups (4 and 5) is reported.
REGIOSELECTIVITY IN THE 1,3-DIPOLAR CYCLOADDITION OF NITRILE OXIDES TO ALKYLIDENECYCLOPROPANES.
Brandi, Alberto,Carli, Silvio,Guarna, Antonio,Sarlo, Francesco De
, p. 3845 - 3848 (2007/10/02)
The 1,3-dipolar cycloaddition of nitrile oxides to methylenecyclopropanes substituted on the exocyclic double bond gives prevalently or exclusively 4-spirocyclopropane isoxazolines when the substituent is arylic or alkylic group, 5-spirocyclopropane isoxa
