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• W2952113856 abstract "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‐2 H ‐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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• W2952113856 date "2011-04-12" @default.
• W2952113856 modified "2023-10-18" @default.
• W2952113856 title "Synthesis of dispiro[oxindole-pyrrolidine]-thiazolo[3,2-a][1,3,5]triazines by 1,3-dipolar cycloaddition" @default.
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• W2952113856 doi "https://doi.org/10.1002/jhet.647" @default.
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