A series of new 3a',6a'-dihydro-2'H-spiro[indole-3,1'-pyrrolo[3,4-c]pyrrole]-2,4',6'(1H,3'H,5'H)- triones has been synthesized by cycloaddition of azomethine ylides, obtained from isatins and acyclic aliphatic and sulfur-containing α-amino acids, to maleimides. The direction of the cycloaddition was determined and the chemical properties of the obtained spiro products were examined.
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Here and subsequently, * in the description of compounds 5a-v, 6a,b indicates what alcohol was used in the synthesis.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 945-960, June, 2013.
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Pavlovskaya, T.L., Red’kin, R.G., Yaremenko, F.G. et al. Synthesis and chemical properties of new derivatives of 3a',6a'-dihydro-2'H-spiro- [indole-3,1'-pyrrolo[3,4-c]pyrrole]-2,4',6'(1H,3'H,5'H)-trione. Chem Heterocycl Comp 49, 882–896 (2013). https://doi.org/10.1007/s10593-013-1322-1
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DOI: https://doi.org/10.1007/s10593-013-1322-1