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N-Heterocyclic carbene-catalyzed oxidative [3 + 2] annulation of dioxindoles and enals: cross coupling of homoenolate and enolate
Open accessAbstract
The N-heterocyclic carbene-catalyzed oxidative [3 + 2] annulation of dioxindole and enals was developed, giving the corresponding spirocyclic oxindole-γ-lactones in good yields with high to excellent diastereo- and enantioselectivities.
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Citations
Cited by
Catalytic asymmetric synthesis of spirooxindoles: recent developments
Mei, G.-J., & Shi, F. (2018) · Chemical Communications · doi:10.1039/c8cc02364f · Cited by 467
Recent advances in N-heterocyclic carbene-based radical catalysis
Ishii, T., Nagao, K., & Ohmiya, H. (2020) · Chemical Science · doi:10.1039/d0sc01538e · Cited by 394
Chen, X.-Y., Gao, Z.-H., & Ye, S. (2020) · Accounts of Chemical Research · doi:10.1021/acs.accounts.9b00635 · Cited by 386
Self-citationN-Heterocyclic Carbene-Catalyzed Decarboxylative Alkylation of Aldehydes
Ishii, T., Kakeno, Y., Nagao, K., & Ohmiya, H. (2019) · Journal of the American Chemical Society · doi:10.1021/jacs.9b00880 · Cited by 336
Liu, K., Schwenzer, M., & Studer, A. (2022) · ACS Catalysis · doi:10.1021/acscatal.2c03996 · Cited by 325
Metadata
- Authors
- Chen, X.-Y., Chen, K.-Q., Sun, D.-Q., & Ye, S.
- Venue
- Chemical Science
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2017
- Volume
- 8
- Issue
- 3
- Pages
- 1936-1941
- ISSN
- 2041-6520 (ISSN-L)
- 2041-6539
- OpenAlex
- W2553736986
- Cited by
- 159
- References
- 0
- FWCI
- 8.02
- Type
- journal article
- Language
- en
- Open access
- diamond
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- Chen, X.-Y., Chen, K.-Q., Sun, D.-Q., & Ye, S. (2017). N-Heterocyclic carbene-catalyzed oxidative [3 + 2] annulation of dioxindoles and enals: cross coupling of homoenolate and enolate. Chemical Science. https://doi.org/10.1039/c6sc04135c
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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.
