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- W1979943997 abstract "The 1,3-dipolar cycloaddition of an azomethine ylide generated by a decarboxylative route from sarcosine and isatin to 7-arylmethylidene-3-aryl-3,4-dihydro-2H-thiazolo[3,2-a][1,3,5]triazin-6(7H)-ones afforded novel dispiro[oxindole-pyrrolidine]-thiazolo[3,2-a][1,3,5]triazines in moderate yields. The structures of the products were determined and characterized thoroughly by NMR, MS, IR, and elemental analysis. The results of experiment indicated that this 1,3-dipolar cycloaddition proceeded with high stereoselectivity and regioselectivity. J. Heterocyclic Chem., (2011)." @default.
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- W1979943997 date "2011-11-17" @default.
- W1979943997 modified "2023-09-26" @default.
- W1979943997 title "ChemInform Abstract: Synthesis of Dispiro[oxindole-pyrrolidine]-thiazolo[3,2-a][1,3,5]triazines by 1,3-Dipolar Cycloaddition." @default.
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- W1979943997 doi "https://doi.org/10.1002/chin.201150157" @default.
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