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- W2952366722 endingPage "9100" @default.
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- W2952366722 abstract "1,3-Dipolar cycloaddition reaction of sydnone-N-ylides, as model bis(1,3-dipoles), with acetylenic dipolarophiles in 1,2-epoxybutane under reflux gave exclusively pyrroloazines containing a sydnone moiety that resulted by preferred reaction of the N-ylide 1,3-dipole with the acetylenic dipolarophiles. The assembled sydnone-ylide hybrid structures were generated in situ from N-heteroaromatic bromides. The structure of the new compounds was assigned by IR and NMR spectroscopy and confirmed by X-ray analysis for a representative compound." @default.
- W2952366722 created "2019-06-27" @default.
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- W2952366722 date "2015-12-01" @default.
- W2952366722 modified "2023-10-18" @default.
- W2952366722 title "1,3-Dipolar cycloaddition between acetylenic dipolarophiles and sydnone-N-ylides as bis(1,3-dipoles)" @default.
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- W2952366722 doi "https://doi.org/10.1016/j.tet.2015.10.021" @default.
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