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October 30, 2012Chemistry - A European Journal85 citationsOpen Access

Highly Enantio‐ and Diastereoselective Generation of Two Quaternary Centers in Spirocyclopropanation of Oxindole Derivatives.

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ANArtur NooleNSNatalia SucmanMKMikhail Kabeshov

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Abstract

Spirocyclopropanes: Only one out of eight possible stereoisomers was obtained in the asymmetric cascade cyclopropanation of alkylidene oxindoles with ethyl 2-chloroacetoacetate. Improved catalyst design ensured that spirocyclopropyl oxindoles featuring two quaternary centers were synthesized in high yield and high enantio- and diastereoselectivity (see scheme).

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Cite This Study

Noole et al. (2012) studied this question.

synapsesocial.com/papers/69d9ab070d540cafc5836d59https://doi.org/10.1002/chem.201203099
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