4.4 Article

Regioselective synthesis of spiro isoxazole-oxindole-tetrahydrothiophene hybrids via cascade reactions under catalyst-free conditions

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JOURNAL OF HETEROCYCLIC CHEMISTRY
卷 57, 期 1, 页码 469-476

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WILEY
DOI: 10.1002/jhet.3803

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  1. Science and Engineering Research Board [SB/FT/CS -136/2012]
  2. Science for Equity, Empowerment and Development Division [SB/EMEQ -103/2014]

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Catalyst-free synthesis of the isoxazole-spirooxindole-tetrahydrothiophene hybrids is reported. Formation of 1,4-thia-Michael and intramolecular aldol reactions were observed (instead of 1,6-thia-Michael followed by vinylogous Henry reactions) in a regioselective fashion to give new isoxazole-spirooxindole-tetrahydrothiophene hybrids with excellent yields.

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