The DOI matches its Crossref record; 46 of the 46 references it cites were found in a registry or an index.
N‐Heterocyclic Carbene Catalysis via Azolium Dienolates: An Efficient Strategy for Remote Enantioselective Functionalizations
Abstract
N‐heterocyclic carbene (NHC) catalysis has emerged as a powerful strategy in organic synthesis. In recent years a number of reviews have been published on NHC‐catalyzed transformations involving Breslow intermediates, acyl azoliums, α,β‐unsaturated acyl azoliums, homoenolate equivalents, and azolium enolates. However, the azolium dienolate intermediates generated by NHCs have been employed in asymmetric synthesis only very recently, especially in cycloadditions dealing with remote functionalization. This Minireview highlights all the developments and the new advances in NHC‐catalyzed asymmetric cycloaddition reactions involving azolium dienolate intermediates.
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Cites
An overview of N-heterocyclic carbenes
Hopkinson, M. N., Richter, C., Schedler, M., & Glorius, F. (2014) · Nature · doi:10.1038/nature13384 · Cited by 4,264
Organocatalysis by N-Heterocyclic Carbenes
Enders, D., Niemeier, O., & Henseler, A. (2007) · Chemical Reviews · doi:10.1021/cr068372z · Cited by 3,059
Self-citationOrganocatalytic Reactions Enabled by N-Heterocyclic Carbenes
Flanigan, D. M., Romanov-Michailidis, F., White, N. A., & Rovis, T. (2015) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00060 · Cited by 2,045
On the Mechanism of Thiamine Action. IV.1 Evidence from Studies on Model Systems
Breslow, R. (1958) · Journal of the American Chemical Society · doi:10.1021/ja01547a064 · Cited by 1,721
Organocatalytic umpolung: N-heterocyclic carbenes and beyond
Bugaut, X., & Glorius, F. (2012) · Chemical Society Reviews · doi:10.1039/c2cs15333e · Cited by 1,394
Nucleophilic Carbenes in Asymmetric Organocatalysis
Enders, D., & Balensiefer, T. (2004) · Accounts of Chemical Research · doi:10.1021/ar030050j · Cited by 1,045
Self-citationN‐Heterocyclic Carbene Catalyzed Domino Reactions
Grossmann, A., & Enders, D. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201105415 · Cited by 987
Self-citationAsymmetric Fluorination, Trifluoromethylation, and Perfluoroalkylation Reactions
Ma, J.-A., & Cahard, D. (2004) · Chemical Reviews · doi:10.1021/cr030143e · Cited by 885
Acyl anion free N-heterocyclic carbene organocatalysis
Ryan, S. J., Candish, L., & Lupton, D. W. (2013) · Chemical Society Reviews · doi:10.1039/c3cs35522e · Cited by 827
Burstein, C., & Glorius, F. (2004) · Angewandte Chemie International Edition · doi:10.1002/anie.200461572 · Cited by 723
Cited by
Chen, X.-Y., Gao, Z.-H., & Ye, S. (2020) · Accounts of Chemical Research · doi:10.1021/acs.accounts.9b00635 · Cited by 386
Self-citationShee, S., Mukherjee, S., Gonnade, R. G., & Biju, A. T. (2020) · Organic Letters · doi:10.1021/acs.orglett.0c01756 · Cited by 34
Metadata
- Authors
- Chen, X., Liu, Q., Chauhan, P., & Enders, D.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2018-03-09
- Volume
- 57
- Issue
- 15
- Pages
- 3862-3873
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2768775773
- Cited by
- 293
- References
- 46
- FWCI
- 11.83
- Type
- journal article
- Language
- en
- Open access
- closed
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- Chen, X., Liu, Q., Chauhan, P., & Enders, D. (2018). N‐Heterocyclic Carbene Catalysis via Azolium Dienolates: An Efficient Strategy for Remote Enantioselective Functionalizations. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201709684
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