Supporting Information
Supporting Information File 1: Experimental section, analytical data (NMR and MS). | ||
Format: PDF | Size: 293.9 KB | Download |
Cite the Following Article
Tertiary alcohol preferred: Hydroxylation of trans-3-methyl-L-proline with proline hydroxylases
Christian Klein and Wolfgang Hüttel
Beilstein J. Org. Chem. 2011, 7, 1643–1647.
https://doi.org/10.3762/bjoc.7.193
How to Cite
Klein, C.; Hüttel, W. Beilstein J. Org. Chem. 2011, 7, 1643–1647. doi:10.3762/bjoc.7.193
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Charlton, S. N.; Hayes, M. A. Oxygenating Biocatalysts for Hydroxyl Functionalisation in Drug Discovery and Development. ChemMedChem 2022, 17, e202200115. doi:10.1002/cmdc.202200115
- Dong, Y.; Schuppe, A. W.; Mai, B. K.; Liu, P.; Buchwald, S. L. Confronting the Challenging Asymmetric Carbonyl 1,2-Addition Using Vinyl Heteroarene Pronucleophiles: Ligand-Controlled Regiodivergent Processes through a Dearomatized Allyl-Cu Species. Journal of the American Chemical Society 2022, 144, 5985–5995. doi:10.1021/jacs.2c00734
- Smart, T. J.; Hamed, R. B.; Claridge, T. D. W.; Schofield, C. J. Studies on the selectivity of proline hydroxylases reveal new substrates including bicycles. Bioorganic chemistry 2019, 94, 103386. doi:10.1016/j.bioorg.2019.103386
- Mattay, J.; Hüttel, W. Pipecolic Acid Hydroxylases: A Monophyletic Clade among cis-Selective Bacterial Proline Hydroxylases that Discriminates l-Proline. Chembiochem : a European journal of chemical biology 2017, 18, 1523–1528. doi:10.1002/cbic.201700187
- Gajare, V.; Khobare, S. R.; Malavika, B.; Rajana, N.; Rao, B. V.; Kumar, U. K. S. A short diastereoselective synthesis of cis-(2S,4S) and cis-(2R,4R)-4-hydroxyprolines. Tetrahedron Letters 2015, 56, 3743–3746. doi:10.1016/j.tetlet.2015.03.119
- Baud, D.; Saaidi, P.-L.; Monfleur, A.; Harari, M.; Cuccaro, J.; Fossey, A.; Besnard, M.; Debard, A.; Mariage, A.; Pellouin, V.; Petit, J.-L.; Salanoubat, M.; Weissenbach, J.; de Berardinis, V.; Zaparucha, A. Synthesis of Mono‐ and Dihydroxylated Amino Acids with New α‐Ketoglutarate‐Dependent Dioxygenases: Biocatalytic Oxidation of C ? H Bonds. ChemCatChem 2014, 6, 3012–3017. doi:10.1002/cctc.201402498
- Hara, R.; Uchiumi, N.; Okamoto, N.; Kino, K. Regio- and stereoselective oxygenation of proline derivatives by using microbial 2-oxoglutarate-dependent dioxygenases. Bioscience, biotechnology, and biochemistry 2014, 78, 1384–1388. doi:10.1080/09168451.2014.918490
- Müller, M. Enzymatic Synthesis of Tertiary Alcohols. ChemBioEng Reviews 2014, 1, 14–26. doi:10.1002/cben.201300005
- Hüttel, W. Biocatalytic Production of Chemical Building Blocks in Technical Scale with α-Ketoglutarate-Dependent Dioxygenases. Chemie Ingenieur Technik 2013, 85, 809–817. doi:10.1002/cite.201300008
- Müller, M. Biokatalytische Synthesen tertiärer Alkohole. Chemie Ingenieur Technik 2013, 85, 795–808. doi:10.1002/cite.201200210