The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.
Development of Novel Lewis Acid Catalysts for Selective Organic Reactions in Aqueous Media
Abstract
New types of Lewis acids as water-compatible catalysts have been developed. Various metal salts were found to work as Lewis acid catalysts in aqueous media, and catalytic asymmetric aldol reactions in such media have been attained. Furthermore, Lewis acid-surfactant combined catalysts, which can be used for reactions in water without using any organic cosolvents, have been also developed. These investigations will contribute to reducing the use of harmful organic solvents and to develop efficient catalytic systems which cannot be realized in conventional organic solvents.
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Cites
Green Chemistry: Theory and Practice
Anastas, P. T., & Warner, J. C. (1998) · Medical Entomology and Zoology · Cited by 8,599
Comprehensive organic synthesis
Knochel, P., & Molander, G. A. (2014) · Elsevier eBooks · Cited by 6,231
Baes, C. F., & Mesmer, R. E. (1976) · Medical Entomology and Zoology · Cited by 4,657
Comprehensive asymmetric catalysis
Jacobsen, E. N., Pfaltz, A., & 山本, 尚. (1999) · Springer eBooks · Cited by 3,786
Catalysis in micellar and macromolecular systems
Cordes, E. H. (1978) · Journal of Colloid and Interface Science · doi:10.1016/0021-9797(78)90120-0 · Cited by 1,288
Organic reactions in aqueous media
(1998) · Choice Reviews Online · doi:10.5860/choice.35-3311 · Cited by 1,260
Catalysis in micellar and macromolecular systems
Fendler, J. H., & Fendler, E. J. (2012) · Cited by 1,079
Yamakawa, M., Yamada, I., & Noyori, R. (2001) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20010803)40:15<2818::aid-anie2818>3.0.co;2-y · Cited by 404
Evans, D. A., Kozlowski, M. C., Murry, J. A., Burgey, C. S., Campos, K. R., Connell, B. T., & Staples, R. J. (1999) · Journal of the American Chemical Society · doi:10.1021/ja9829822 · Cited by 388
Kobayashi, S., Nagayama, S., & Busujima, T. (1998) · Journal of the American Chemical Society · doi:10.1021/ja980715q · Cited by 378
Self-citation
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Organocatalysis Mediated by (Thio)urea Derivatives
Connon, S. J. (2006) · Chemistry – A European Journal · doi:10.1002/chem.200501076 · Cited by 846
Nb2O5·nH2O as a Heterogeneous Catalyst with Water-Tolerant Lewis Acid Sites
Nakajima, K., Baba, Y., Noma, R., Kitano, M., Kondo, J. N., Hayashi, S., & Hara, M. (2011) · Journal of the American Chemical Society · doi:10.1021/ja110482r · Cited by 577
Activation of Carbonyl-Containing Molecules with Solid Lewis Acids in Aqueous Media
Román-Leshkov, Y., & Davis, M. E. (2011) · ACS Catalysis · doi:10.1021/cs200411d · Cited by 401
Liang, Y., Liu, S., Xia, Y., Li, Y., & Yu, Z. (2008) · Chemistry – A European Journal · doi:10.1002/chem.200701725 · Cited by 369
Krasovskiy, A., Kopp, F., & Knochel, P. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200502485 · Cited by 342
Wang, Y., Wang, F., Song, Q., Xin, Q., Xu, S., & Xu, J. (2013) · Journal of the American Chemical Society · doi:10.1021/ja310498c · Cited by 324
Polymers without Petrochemicals: Sustainable Routes to Conventional Monomers
Hayes, G., Laurel, M., MacKinnon, D., Zhao, T., Houck, H. A., & Becer, C. R. (2023) · Chemical Reviews · doi:10.1021/acs.chemrev.2c00354 · Cited by 253
Guillaume, S. M., & Carpentier, J.-F. (2012) · Catalysis Science & Technology · doi:10.1039/c2cy00507g · Cited by 102
Economical concerns of lignin in the energy sector
Sharma, A., Kaur, P., Singh, G., & Arya, S. K. (2021) · Cleaner Engineering and Technology · doi:10.1016/j.clet.2021.100258 · Cited by 38
Gruszka, W., & Garden, J. A. (2022) · Chemical Communications · doi:10.1039/d1cc06594g · Cited by 20
Metadata
- Authors
- Kobayashi, S., & Manabe, K.
- Venue
- Accounts of Chemical Research
- Publisher
- American Chemical Society (ACS)
- Published
- 2002-02-20
- Volume
- 35
- Issue
- 4
- Pages
- 209-217
- ISSN
- 0001-4842 (ISSN-L)
- 1520-4898
- OpenAlex
- W1998714557
- Cited by
- 771
- References
- 30
- FWCI
- 24.93
- Type
- journal article
- Language
- en
- Open access
- closed
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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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