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Cited by 210

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

An Organocatalytic [3+2] Cyclisation Strategy for the Highly Enantioselective Synthesis of Spirooxindoles

Voituriez, Arnaud, Pinto, Nathalie, Neel, Mathilde, Retailleau, Pascal, Marinetti, Angela·2010·Chemistry – A European Journal

Abstract

Power of P: Phosphine-promoted [3+2] annulation reactions between electron-poor allenes and 3-arylidene indolin-2-ones afford a new organocatalytic strategy for the synthesis of the spirocyclic core of oxindolic cyclopentanes (see scheme). Asymmetric variants of these reactions have been implemented by using chiral catalysts, giving very high levels of asymmetric induction.

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Metadata

Authors
Voituriez, A., Pinto, N., Neel, M., Retailleau, P., & Marinetti, A.
Venue
Chemistry – A European Journal
Publisher
Wiley
Published
2010-09-17
Volume
16
Issue
42
Pages
12541-12544
ISSN
  • 0947-6539 (ISSN-L)
  • 1521-3765
OpenAlex
W2165756524
Cited by
210
References
1
FWCI
13.58
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: An Organocatalytic [3+2] Cyclisation Strategy for the Highly Enantioselective Synthesis of Spirooxindoles. https://app.cochat.ai/papers/10.1002/chem.201001791
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Voituriez, A., Pinto, N., Neel, M., Retailleau, P., & Marinetti, A. (2010). An Organocatalytic [3+2] Cyclisation Strategy for the Highly Enantioselective Synthesis of Spirooxindoles. Chemistry – A European Journal. https://doi.org/10.1002/chem.201001791

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