The DOI matches its Crossref record.
Highly Enantioselective Alkylation Reaction of Enamides by Brønsted-Acid Catalysis
Abstract
The H8-BINOL-derived, phosphoric acid catalyzed, highly enatioselective alkylation reaction of enamides with indolyl alcohols has been described. A phosphoric acid derived from H8-BINOL enabled an asymmetric alpha-alkylation of enamides with indolyl alcohols to give beta-aryl 3-(3-indolyl)propanones in high yields (up to 96%) and with excellent enantioselectivity (up to 96% ee).
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Citations
Cited by
Parmar, D., Sugiono, E., Raja, S., & Rueping, M. (2014) · Chemical Reviews · doi:10.1021/cr5001496 · Cited by 2,118
Dagousset, G., Zhu, J., & Masson, G. (2011) · Journal of the American Chemical Society · doi:10.1021/ja205891m · Cited by 287
Wang, X., Liu, J., Xu, L., Hao, Z., Wang, L., & Xiao, J. (2015) · RSC Advances · doi:10.1039/c5ra21919a · Cited by 28
Metadata
- Authors
- Guo, Q.-X., Peng, Y.-G., Zhang, J.-W., Song, L., Feng, Z., & Gong, L.-Z.
- Venue
- Organic Letters
- Publisher
- American Chemical Society (ACS)
- Published
- 2009-09-11
- Volume
- 11
- Issue
- 20
- Pages
- 4620-4623
- ISSN
- 1523-7052 (ISSN-L)
- 1523-7060
- OpenAlex
- W2081048890
- Cited by
- 238
- References
- 0
- FWCI
- 10.70
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Highly Enantioselective Alkylation Reaction of Enamides by Brønsted-Acid Catalysis. https://app.cochat.ai/papers/10.1021/ol901892s
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- Guo, Q.-X., Peng, Y.-G., Zhang, J.-W., Song, L., Feng, Z., & Gong, L.-Z. (2009). Highly Enantioselective Alkylation Reaction of Enamides by Brønsted-Acid Catalysis. Organic Letters. https://doi.org/10.1021/ol901892s
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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