Synthesis of dispiro[oxindole‐pyrrolidine]‐thiazolo[3,2‐a][1,3,5]triazines by 1,3‐dipolar cycloaddition |
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| Authors: | Xiaofang Li Zhikui Li Aiting Zheng Guobin Li Xianyong Yu Pinggui Yi |
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| Institution: | Key Laboratory of Theoretical Chemistry and Molecular Simulation of Ministry of Education, Hunan Province College Key Laboratory of QSAR/QSPR, School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan, Hunan 411201, China |
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| 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‐thiazolo3,2‐a]1,3,5]triazin‐6(7H)‐ones afforded novel dispirooxindole‐pyrrolidine]‐thiazolo3,2‐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). |
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