The DOI matches its Crossref record; 36 of the 36 references it cites were found in a registry or an index.
Biocatalysis — key to sustainable industrial chemistry
Abstract
The ongoing trends to process improvements, cost reductions and increasing quality, safety, health and environment requirements of industrial chemical transformations have strengthened the translation of global biocatalysis research work into industrial applications. One focus has been on biocatalytic single-step reactions with one or two substrates, the identification of bottlenecks and molecular as well as engineering approaches to overcome these bottlenecks. Robust industrial procedures have been established along classes of biocatalytic single-step reactions. Multi-step reactions and multi-component reactions (MCRs) enable a bottom-up approach with biocatalytic reactions working together in one compartment and recations hindering each other within different compartments or steps. The understanding of the catalytic functions of known and new enzymes is key for the development of new sustainable chemical transformations.
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Cites
Biocatalytic Asymmetric Synthesis of Chiral Amines from Ketones Applied to Sitagliptin Manufacture
Savile, C. K., Janey, J. M., Mundorff, E. C., Moore, J. C., Tam, S., Jarvis, W. R., Colbeck, J. C., Krebber, A., Fleitz, F. J., Brands, J., et al. (2010) · Science · doi:10.1126/science.1188934 · Cited by 1,756
Green chemistry for chemical synthesis
Li, C.-J., & Trost, B. M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804348105 · Cited by 940
Protecting-group-free synthesis as an opportunity for invention
Young, I. S., & Baran, P. S. (2009) · Nature Chemistry · doi:10.1038/nchem.216 · Cited by 667
Synthesis at the molecular frontier
Wender, P. A., & Miller, B. L. (2009) · Nature · doi:10.1038/460197a · Cited by 579
Advances in the Biology and Chemistry of Sialic Acids
Chen, X., & Varki, A. (2010) · ACS Chemical Biology · doi:10.1021/cb900266r · Cited by 543
Natural Products Version 2.0: Connecting Genes to Molecules
Walsh, C. T., & Fischbach, M. A. (2010) · Journal of the American Chemical Society · doi:10.1021/ja909118a · Cited by 468
A green-by-design biocatalytic process for atorvastatin intermediate
Ma, S. K., Gruber, J., Davis, C., Newman, L., Gray, D., Wang, A., Grate, J., Huisman, G. W., & Sheldon, R. A. (2010) · Green Chem. · doi:10.1039/b919115c · Cited by 440
ω-Transaminases for the synthesis of non-racemic α-chiral primary amines
Koszelewski, D., Tauber, K., Faber, K., & Kroutil, W. (2010) · Trends in Biotechnology · doi:10.1016/j.tibtech.2010.03.003 · Cited by 427
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Practical chiral alcohol manufacture using ketoreductases
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Cited by
Enzyme immobilisation in biocatalysis: why, what and how
Sheldon, R. A., & van Pelt, S. (2013) · Chem. Soc. Rev. · doi:10.1039/c3cs60075k · Cited by 2,675
Bioeconomy for sustainable development
Aguilar, A., Twardowski, T., & Wohlgemuth, R. (2019) · Biotechnology Journal · doi:10.1002/biot.201800638 · Cited by 206
Self-citation
Metadata
- Authors
- Wohlgemuth, R.
- Venue
- Current Opinion in Biotechnology
- Publisher
- Elsevier BV
- Published
- 2010-12
- Volume
- 21
- Issue
- 6
- Pages
- 713-724
- ISSN
- 0958-1669 (ISSN-L)
- OpenAlex
- W2077962142
- Cited by
- 334
- References
- 36
- FWCI
- 1.15
- Type
- journal article
- Language
- en
- Open access
- closed
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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.