The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Organocatalytic Asymmetric Aza‐Michael Additions
Abstract
The catalytic aza‐Michael addition is an important reaction within synthetic organic chemistry, given the significance of the biologically and synthetically interesting products, such as β‐amino acids and β‐lactams. In the last decade organocatalysis emerged as a powerful tool in asymmetric synthesis and had a large impact on the development of asymmetric and catalytic conjugate additions of nitrogen nucleophiles to Michael acceptors. In this review a first summary of the recent rapid progress of asymmetric organocatalyzed aza‐Michael reactions is presented.
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Cites
Lin, Q., Meloni, D., Pan, Y., Xia, M., Rodgers, J., Shepard, S., Li, M., Galya, L., Metcalf, B., Yue, T.-Y., et al. (2009) · Organic Letters · doi:10.1021/ol900350k · Cited by 171
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Parmar, D., Sugiono, E., Raja, S., & Rueping, M. (2014) · Chemical Reviews · doi:10.1021/cr5001496 · Cited by 2,118
Fèvre, M., Pinaud, J., Gnanou, Y., Vignolle, J., & Taton, D. (2013) · Chemical Society Reviews · doi:10.1039/c2cs35383k · Cited by 532
Metadata
- Authors
- Enders, D., Wang, C., & Liebich, J. X.
- Venue
- Chemistry – A European Journal
- Publisher
- Wiley
- Published
- 2009-10-20
- Volume
- 15
- Issue
- 42
- Pages
- 11058-11076
- ISSN
- 0947-6539 (ISSN-L)
- 1521-3765
- OpenAlex
- W2079568090
- Cited by
- 474
- References
- 1
- FWCI
- 22.03
- Type
- journal article
- Language
- en
- Open access
- closed
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- Enders, D., Wang, C., & Liebich, J. X. (2009). Organocatalytic Asymmetric Aza‐Michael Additions. Chemistry – A European Journal. https://doi.org/10.1002/chem.200902236
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