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Synthesis of new spiroheterocycles-fused isoxazoline from 2-arylidenes-3-phenyl-1-indanones through a regio-and diastereospecific 1,3-dipolar cycloaddition

Asmae Mahfoud, Abdelali Kerbal, Asmae Nakkabi, Mohamed El Yazidi, Mohamed Akhazzane, Mohamed Bakhouch, Youssra Kanzouai, Rachid Bouzammit, Ghali Al Houari

Abstract


New spiroisoxazolines 3 have been synthesized by 1,3-dipolar cycloaddition of arylnitrile oxides with 2-arylidenes-3-phenyl-1-indanones. The reaction occurs in a regiospecific and diastereospecific manner and leads to one cycloadduct in all the cases. The proposed structure of the obtained cycloadducts was established based on spectroscopic data and confirmed by radiocrystallographic study. The spectral data were in favor of the observed regiochemistry and diastereoselectivity of this reaction.


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DOI: http://dx.doi.org/10.13171/mjc02105141076gh

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