Efficient synthesis of novel spiro[indole-3,6′-pyrano[2,3-d][1,3]thiazolo[3,2-a]pyrimidine derivatives through an organobase-catalyzed, three-component reaction
A fast and convenient protocol for the synthesis of novel spirooxindole derivatives in excellent yields was developed by the three-component reactions of malononitrile, isatin, and 2,3-dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidine-5,7(6H)-dione in the presence of diisopropylethylamine. [Display omitted]
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Published in: | Tetrahedron Vol. 71; no. 16; pp. 2458 - 2462 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Elsevier Ltd
22-04-2015
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Subjects: | |
Online Access: | Get full text |
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Summary: | A fast and convenient protocol for the synthesis of novel spirooxindole derivatives in excellent yields was developed by the three-component reactions of malononitrile, isatin, and 2,3-dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidine-5,7(6H)-dione in the presence of diisopropylethylamine.
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ISSN: | 0040-4020 1464-5416 |
DOI: | 10.1016/j.tet.2015.01.055 |