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Diels_Alder reactions in water
Open accessAbstract
This review illustrates how water, as an environmentally friendly solvent, can have significant additional benefits when it is used as a solvent for the Diels_Alder reaction. The mechanism by which the unique properties of water enhance the rate and selectivity are discussed. Also, possibilities for the achievement of further increases in rate and enantioselectivity of aqueous Diels_Alder reactions through Lewis-acid and micellar catalysis are reviewed.
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Citations
Cited by
Stereoselective Organic Reactions in Water
Lindström, U. M. (2002) · Chemical Reviews · doi:10.1021/cr010122p · Cited by 1,642
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Ramamurthy, V., & Sivaguru, J. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00040 · Cited by 459
Surfactant Assemblies and their Various Possible Roles for the Origin(S) of Life
Walde, P. (2006) · Origins of Life and Evolution of Biospheres · doi:10.1007/s11084-005-9004-3 · Cited by 138
Metadata
- Authors
- Otto, S., & Engberts, J. B. F. N.
- Venue
- Pure and Applied Chemistry
- Publisher
- Walter de Gruyter GmbH
- Published
- 2000-01-01
- Volume
- 72
- Issue
- 7
- Pages
- 1365-1372
- ISSN
- 0033-4545 (ISSN-L)
- 1365-3075
- OpenAlex
- W2138886056
- Cited by
- 208
- References
- 0
- FWCI
- 4.94
- Type
- journal article
- Language
- en
- Open access
- hybrid
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- Otto, S., & Engberts, J. B. F. N. (2000). Diels_Alder reactions in water. Pure and Applied Chemistry. https://doi.org/10.1351/pac200072071365
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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.