The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Enantioselective Michael Reaction of Malonates to Nitroolefins Catalyzed by Bifunctional Organocatalysts
Abstract
Michael reaction of malonates to nitroolefins with chiral bifunctional organocatalysts, bearing both a thiourea and tertiary amino group, afforded Michael adducts with high yields and enantioselectivities (up to 95%, up to 93% ee).
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Citations
Cites
First Synthesis of a β2-Homoamino Acid by Enantioselective Catalysis
Rimkus, A., & Sewald, N. (2003) · Organic Letters · doi:10.1021/ol027252k · Cited by 98
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Metadata
- Authors
- Okino, T., Hoashi, Y., & Takemoto, Y.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2003-09-30
- Volume
- 125
- Issue
- 42
- Pages
- 12672-12673
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W1995396482
- Cited by
- 1,430
- References
- 1
- FWCI
- 27.00
- Type
- journal article
- Language
- en
- Open access
- closed
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- The paper
- Okino, T., Hoashi, Y., & Takemoto, Y. (2003). Enantioselective Michael Reaction of Malonates to Nitroolefins Catalyzed by Bifunctional Organocatalysts. Journal of the American Chemical Society. https://doi.org/10.1021/ja036972z
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
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.
