The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Asymmetric Two‐Center Catalysis—Learning from Nature
Abstract
In spite of relatively few examples, two-center catalysis is proving to be a clever and effective means of performing diverse reactions with both high regio- and enantioselectivity. A simple scheme allows classification of the efficient M1–M2–binol complexes 1 as well as the enzymes urease and carbon monoxide dehydrogenase. M1 = La, Al,…; M2 = Li, Na, K,….
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Citations
Cites
Noyori, R., & Kitamura, M. (1991) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199100491 · Cited by 1,214
Cited by
Material Applications for Salen Frameworks
Wezenberg, S. J., & Kleij, A. W. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200702468 · Cited by 289
Metadata
- Authors
- Steinhagen, H., & Helmchen, G.
- Venue
- Angewandte Chemie International Edition in English
- Publisher
- Wiley
- Published
- 1996-11
- Volume
- 35
- Issue
- 20
- Pages
- 2339-2342
- ISSN
- 0570-0833 (ISSN-L)
- OpenAlex
- W2114858685
- Cited by
- 248
- References
- 1
- FWCI
- 9.27
- Type
- journal article
- Language
- en
- Open access
- closed
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- Steinhagen, H., & Helmchen, G. (1996). Asymmetric Two‐Center Catalysis—Learning from Nature. Angewandte Chemie International Edition in English. https://doi.org/10.1002/anie.199623391
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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.
