The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Cinchona alkaloid-based phosphoramide catalyzed highly enantioselective Michael addition of unprotected 3-substituted oxindoles to nitroolefins
Abstract
A newly developed cinchonidine-derived phosphoramide 6b, simple and easily available, was identified as a powerful catalyst for the highly enantioselective Michael addition of both unprotected 3-aryl and 3-alkyloxindoles to β-substituted nitroalkenes to furnish the C3 quaternary stereogenic carbon center with an adjacent tertiary stereocenter in up to 21 : 1 diastereoselectivity and up to 99% enantioselectivity.
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Citations
Cites
Green Chemistry: Principles and Practice
Anastas, P., & Eghbali, N. (2010) · Chem. Soc. Rev. · doi:10.1039/b918763b · Cited by 5,256
Cited by
Recent advances in organocatalytic methods for the synthesis of disubstituted 2- and 3-indolinones
Dalpozzo, R., Bartoli, G., & Bencivenni, G. (2012) · Chemical Society Reviews · doi:10.1039/c2cs35100e · Cited by 673
Metadata
- Authors
- Ding, M., Zhou, F., Liu, Y.-L., Wang, C.-H., Zhao, X.-L., & Zhou, J.
- Venue
- Chemical Science
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2011
- Volume
- 2
- Issue
- 10
- Pages
- 2035
- ISSN
- 2041-6520 (ISSN-L)
- 2041-6539
- OpenAlex
- W2074683026
- Cited by
- 171
- References
- 1
- FWCI
- 11.82
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Cinchona alkaloid-based phosphoramide catalyzed highly enantioselective Michael addition of unprotected 3-substituted oxindoles to nitroolefins. https://app.cochat.ai/papers/10.1039/c1sc00390a
- The paper
- Ding, M., Zhou, F., Liu, Y.-L., Wang, C.-H., Zhao, X.-L., & Zhou, J. (2011). Cinchona alkaloid-based phosphoramide catalyzed highly enantioselective Michael addition of unprotected 3-substituted oxindoles to nitroolefins. Chemical Science. https://doi.org/10.1039/c1sc00390a
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
