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


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Article Info

DATE

2012-08

AUTHORS

A. A. Shvets, Yu. V. Nelyubina, K. A. Lyssenko, S. V. Kurbatov

ABSTRACT

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.

PAGES

1659-1662

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-012-0227-y

DOI

http://dx.doi.org/10.1007/s11172-012-0227-y

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1037447350


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