The DOI matches its Crossref record; 16 of the 16 references it cites were found in a registry or an index.
Toward efficient asymmetric hydrogenation: Architectural and functional engineering of chiral molecular catalysts
Open accessAbstract
Asymmetric hydrogenation uses inexpensive, clean hydrogen gas and a very small amount of a chiral molecular catalyst, providing the most powerful way to produce a wide array of enantio-enriched compounds in a large quantity without forming any waste. The recent revolutionary advances in this field have entirely changed the synthetic approach to producing performance chemicals that require a high degree of structural precision. The means of developing efficient asymmetric hydrogenations is discussed from a mechanistic point of view.
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Citations
Cites
Asymmetric Catalysis: Science and Opportunities (Nobel Lecture 2001)
Noyori, R. (2003) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.200390002 · Cited by 1,870
Self-citationBINAP: an efficient chiral element for asymmetric catalysis
Noyori, R., & Takaya, H. (1990) · Accounts of Chemical Research · doi:10.1021/ar00178a005 · Cited by 1,323
Self-citationNoyori, R., Ohkuma, T., Kitamura, M., Takaya, H., Sayo, N., Kumobayashi, H., & Akutagawa, S. (1987) · Journal of the American Chemical Society · doi:10.1021/ja00253a051 · Cited by 766
Self-citationSandoval, C. A., Ohkuma, T., Muñiz, K., & Noyori, R. (2003) · Journal of the American Chemical Society · doi:10.1021/ja030272c · Cited by 628
Self-citationStereoselective Organic Synthesis via Dynamic Kinetic Resolution
Noyori, R., Tokunaga, M., & Kitamura, M. (1995) · Bulletin of the Chemical Society of Japan · doi:10.1246/bcsj.68.36 · Cited by 531
Self-citationHalide Effects in Transition Metal Catalysis
Fagnou, K., & Lautens, M. (2002) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20020104)41:1<26::aid-anie26>3.0.co;2-9 · Cited by 521
Ohkuma, T., Koizumi, M., Doucet, H., Pham, T., Kozawa, M., Murata, K., Katayama, E., Yokozawa, T., Ikariya, T., & Noyori, R. (1998) · Journal of the American Chemical Society · doi:10.1021/ja983257u · Cited by 409
Self-citationHighly Enantioselective Rh-Catalyzed Hydrogenation Reactions Based on Chiral Monophosphite Ligands
Reetz, M. T., & Mehler, G. (2000) · Angewandte Chemie · doi:10.1002/1521-3773(20001103)39:21<3889::aid-anie3889>3.0.co;2-t · Cited by 377
Ohkuma, T., Koizumi, M., Muñiz, K., Hilt, G., Kabuto, C., & Noyori, R. (2002) · Journal of the American Chemical Society · doi:10.1021/ja026136+ · Cited by 308
Self-citationAsymmetric Catalysis on Industrial Scale: Challenges, Approaches and Solutions
(2003) · Wiley eBooks · doi:10.1002/3527602151 · Cited by 278
Cited by
Enatiomerically pure hydroxycarboxylic acids: current approaches and future perspectives
Ren, Q., Ruth, K., Thöny-Meyer, L., & Zinn, M. (2010) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-010-2530-6 · Cited by 113
Bacterial Poly(hydroxyalkanoates) as a Source of Chiral Hydroxyalkanoic Acids
Ren, Q., Grubelnik, A., Hoerler, M., Ruth, K., Hartmann, R., Felber, H., & Zinn, M. (2005) · Biomacromolecules · doi:10.1021/bm050187s · Cited by 106
Metadata
- Authors
- Noyori, R., Kitamura, M., & Ohkuma, T.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2004-03-19
- Volume
- 101
- Issue
- 15
- Pages
- 5356-5362
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W1508200337
- Cited by
- 277
- References
- 16
- FWCI
- 9.67
- Type
- journal article
- Language
- en
- Open access
- green
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- Noyori, R., Kitamura, M., & Ohkuma, T. (2004). Toward efficient asymmetric hydrogenation: Architectural and functional engineering of chiral molecular catalysts. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.0307928100
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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.
