The DOI matches its Crossref record; 23 of the 23 references it cites were found in a registry or an index.
Targeting Structural and Stereochemical Complexity by Organocascade Catalysis: Construction of Spirocyclic Oxindoles Having Multiple Stereocenters
Abstract
Not so complex: The asymmetric one-step construction of multiple stereocenters in complex spirocyclic oxindoles was achieved with very high fidelity by using distinct organocascade reactions utilizing two organocatalysts, each activating different carbonyl compounds (see scheme; TMS=trimethylsilyl). The complementary approaches demonstrate the potential of organocascade catalysis to face challenging synthetic problems.
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Citations
Cites
Natural products as sources of new drugs over the last 25 years
Newman, D. J., & Cragg, G. M. (2007) · Journal of Natural Products · doi:10.1021/np068054v · Cited by 5,517
Galliford, C. V., & Scheidt, K. A. (2007) · Angewandte Chemie International Edition · doi:10.1002/anie.200701342 · Cited by 2,429
Cascade Reactions in Total Synthesis
Nicolaou, K. C., Edmonds, D. J., & Bulger, P. G. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200601872 · Cited by 2,101
Asymmetric Organocatalytic Domino Reactions
Enders, D., Grondal, C., & Hüttl, M. R. M. (2007) · Angewandte Chemie International Edition · doi:10.1002/anie.200603129 · Cited by 1,624
Asymmetric Aminocatalysis—Gold Rush in Organic Chemistry
Melchiorre, P., Marigo, M., Carlone, A., & Bartoli, G. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200705523 · Cited by 1,256
Self-citationThe ying and yang of asymmetric aminocatalysis
List, B. (2006) · Chemical Communications · doi:10.1039/b514296m · Cited by 824
Inhibiting the p53–MDM2 interaction: an important target for cancer therapy
Chène, P. (2003) · Nature Reviews Cancer · doi:10.1038/nrc991 · Cited by 765
Structure-based design of potent non-peptide MDM2 inhibitors
Ding, K., Lu, Y., Nikolovska-Coleska, Z., Qiu, S., Ding, Y., Gao, W., Stuckey, J., Krajewski, K., Roller, P. P., Tomita, Y., et al. (2005) · Journal of the American Chemical Society · doi:10.1021/ja051147z · Cited by 657
Kaskadenreaktionen in der Totalsynthese
Nicolaou, K. C., Edmonds, D. J., & Bulger, P. G. (2006) · Angewandte Chemie · doi:10.1002/ange.200601872 · Cited by 634
Asymmetrische organokatalytische Dominoreaktionen
Enders, D., Grondal, C., & Hüttl, M. R. M. (2007) · Angewandte Chemie · doi:10.1002/ange.200603129 · Cited by 575
Metadata
- Authors
- Bencivenni, G., Wu, L., Mazzanti, A., Giannichi, B., Pesciaioli, F., Song, M., Bartoli, G., & Melchiorre, P.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2009-09-09
- Volume
- 48
- Issue
- 39
- Pages
- 7200-7203
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2120435976
- Cited by
- 448
- References
- 23
- FWCI
- 28.10
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Targeting Structural and Stereochemical Complexity by Organocascade Catalysis: Construction of Spirocyclic Oxindoles Having Multiple Stereocenters. https://app.cochat.ai/papers/10.1002/anie.200903192
- The paper
- Bencivenni, G., Wu, L., Mazzanti, A., Giannichi, B., Pesciaioli, F., Song, M., Bartoli, G., & Melchiorre, P. (2009). Targeting Structural and Stereochemical Complexity by Organocascade Catalysis: Construction of Spirocyclic Oxindoles Having Multiple Stereocenters. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.200903192
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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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