SYNTHESIS OF DISPIRO[1-BENZOTHIOPHENE-2,3'-PYRROLIDINE- 2',3''-INDOLINE]-2'',3-DIONES IN CYCLOADDITION REACTION
DOI:
https://doi.org/10.1007/5119Keywords:
azomethine ylide, 1-benzothiophen-3(2H)-one, isatin, sarcosine, 1, 3-dipolar cycloaddition.Abstract
The 1,3-dipolar cycloaddition of azomethine ylides derived from isatin and sarcosine to (Z)-2-(arylmethylidene)-1-benzothiophen-3(2H)-ones afforded novel dispiro[1-benzothiophene-2,3'-pyrrolidine-2',3''-indoline]-2'',3-diones in moderate yields. The structures of all the products were characterized by NMR, IR, HRMS together with X-ray crystallographic analysis. The reaction gives two diastereomeric products. This result is different from the cycloaddition of isatin, sarcosine, and other exocyclic olefins which generally afford only oneproduct.
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Published
2019-11-12
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Original Papers