Wolf-Dieter Fessner
Affiliations: | 1993-1998 | Rheinisch-Westfaelische Technische Hochschule, Aachen, NRW, Germany | |
| 1998- | Technische Universität Darmstadt |
Area:
Organic chemistryWebsite:
http://www.chemie.tu-darmstadt.de/fessner/agfessner/lebenslauf/lebenslauf_s02.en.jspGoogle:
"Wolf-Dieter Fessner"Mean distance: 6.58 | S | N | B | C | P |
Parents
Sign in to add mentor| Horst Prinzbach | grad student | 1986 | Universität Freiburg | |
| (Synthese und Chemie hochsymmetrischer Polyquinane: D2h-Pagodan I1h-Dodecahedran D3-Trishomocubantrion [Dh-Pagodan - Ih-Dodecahedran D-Trishomocubantrion]) | ||||
| George M. Whitesides | post-doc | 1986-1987 | Harvard | |
| György Oláh | post-doc | 1988 | USC | |
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Publications
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| Fessner WD, Mertsch A, He N, et al. (2020) An α2,3-sialyltransferase from Photobacterium phosphoreum with broad substrate scope: Controlling hydrolytic activity by directed evolution. Chemistry (Weinheim An Der Bergstrasse, Germany) |
| Hecquet L, Casajus H, Lagarde A, et al. (2020) Enzymatic Synthesis of Aliphatic Acyloins Catalyzed by Thermostable Transketolase Chemcatchem |
| Lorillière M, Guérard‐Hélaine C, Gefflaut T, et al. (2020) Convergent in situ Generation of Both Transketolase Substrates via Transaminase and Aldolase Reactions for Sequential One‐Pot, Three‐Step Cascade Synthesis of Ketoses Chemcatchem. 12: 812-817 |
| Roldán R, Hernández K, Joglar J, et al. (2019) Aldolase-Catalyzed Asymmetric Synthesis of N-Heterocycles by Addition of Simple Aliphatic Nucleophiles to Aminoaldehydes. Advanced Synthesis & Catalysis. 361: 2673-2687 |
| L'enfant M, Bruna F, Lorillière M, et al. (2019) One‐Pot Cascade Synthesis of (3S)‐Hydroxyketones Catalyzed by Transketolase via Hydroxypyruvate Generated in Situ from d‐Serine by d‐Amino Acid Oxidase Advanced Synthesis & Catalysis. 361: 2550-2558 |
| Roldán R, Hernandez K, Joglar J, et al. (2018) Biocatalytic Aldol Addition of Simple Aliphatic Nucleophiles to Hydroxyaldehydes. Acs Catalysis. 8: 8804-8809 |
| Fessner WD, Junker S, Roldan R, et al. (2018) Complete switch of reaction specificity of an aldolase by directed evolution in vitro: Synthesis of generic aliphatic aldol products. Angewandte Chemie (International Ed. in English) |
| Saravanan T, Junker S, Kickstein M, et al. (2017) Donor Promiscuity of a Thermostable Transketolase by Directed Evolution: Efficient Complementation of 1-Deoxy-d-xylulose-5-phosphate Synthase Activity. Angewandte Chemie (International Ed. in English) |
| Roldán R, Sanchez-Moreno I, Scheidt T, et al. (2017) Breaking the dogma of aldolase specificity: Simple aliphatic ketones and aldehyde are nucleophiles for fructose-6-phosphate aldolase. Chemistry (Weinheim An Der Bergstrasse, Germany) |
| Saravanan T, Reif M, Yi D, et al. (2017) Engineering a thermostable transketolase for arylated substrates Green Chemistry. 19: 481-489 |