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- W2572939047 abstract "Triazolyl-2-methylisoxazolidin-3-yl 3-phosphonates have been synthesized by 1,3-dipolar cycloaddition of N-methyl-C-diethoxyphosphorylnitrone and vinyl triazoles. The process showed a complete regioselectivity and a nearly exclusive cis stereoselectivity. M062X/6-31G(d,p) calculations rationalize the regio- and the stereoc hemical results. The formation of a hydrogen bond along a particular reaction channel significan tly stabilizes both transition states and products related to cis -adducts. Biological tests indicate that the obtain ed compounds do not show relevant antiviral and anticancer activity." @default.
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- W2572939047 date "2015-11-25" @default.
- W2572939047 modified "2023-10-17" @default.
- W2572939047 title "5-(3-Phosphonated 1H-1,2,3-triazol-4-yl)isoxazolidines: synthesis, DFT studies and biological properties" @default.
- W2572939047 cites W2605044578 @default.
- W2572939047 doi "https://doi.org/10.3998/ark.5550190.p009.353" @default.
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