Synthesis of bis-spirofused thiapyrrolizidinooxindoles by 1,3-dipolar cycloaddition

The 1,3-dipolar cycloaddition of unstabilized azomethine ylide, which is generated in situ from isatin and thiaproline, to arylidene derivatives of rhodanine affords bis-spirofused thiapyrrolizidinooxindoles. The 1,3-dipolar addition reactions under consideration are fully regio- and diastereoselect...

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Published in:Russian chemical bulletin 2012-08, Vol.61 (8), p.1659-1662
Main Authors: Shvets, A. A., Nelyubina, Yu. V., Lyssenko, K. A., Kurbatov, S. V.
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Language:English
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Chemistry
Chemistry and Materials Science
Chemistry/Food Science
Inorganic Chemistry
Organic Chemistry
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description The 1,3-dipolar cycloaddition of unstabilized azomethine ylide, which is generated in situ from isatin and thiaproline, to arylidene derivatives of rhodanine affords bis-spirofused thiapyrrolizidinooxindoles. The 1,3-dipolar addition reactions under consideration are fully regio- and diastereoselective.
doi_str_mv 10.1007/s11172-012-0227-y
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Chemistry
Chemistry and Materials Science
Chemistry/Food Science
Inorganic Chemistry
Organic Chemistry
title Synthesis of bis-spirofused thiapyrrolizidinooxindoles by 1,3-dipolar cycloaddition
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