Preliminary experiments shows, that [3+2] cycloadditions reactions proceeds with full regioselectivity and high stereoselectivity. In consequence, 3,4-trans-2-methyl-3-(3,4,5-trimethoxyphenyl)-4-halo-4-nitroisoxazolidines are forming as predominantly (or sole) products. Additionally, prognosis for the synthesized compounds to be potential ingredients of drugs is good.
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[3+2] Cycloadditions of 1-halo-1-nitroethenes with (Z)-C-(3,4,5-trimethoxyphenyl)-N-methyl-nitrone as regio- and stereocontrolled source of novel bioactive compounds: preliminary studies Pages 123-128
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Authors: Radomir Jasiński, Ewa Dresler, Maria Mikulska, Daniel Polewski
Keywords: Cycloaddition, Nitroalkenes, Nitrones, Reactivity, Regioselectivity
Abstract:
Journal: CCL | Year: 2016 | Volume: 5 | Issue: 3 | Views: 2004 | Reviews: 0