430 results on '"Griengl, Herfried"'
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2. Biocatalytic Applications of Hydroxynitrile Lyases
3. α- and β-oxygenated aldehydes derived from Diels–Alder reactions as substrates for hydroxynitrile lyases
4. De novo synthesis of pentoses via cyanohydrins as key intermediates
5. Investigation of lipase-catalyzed Michael-type carbon–carbon bond formations
6. Four types of threonine aldolases: Similarities and differences in kinetics/thermodynamics
7. Potential and capabilities of hydroxynitrile lyases as biocatalysts in the chemical industry
8. Counteracting expression deficiencies by anticipating posttranslational modification of PaHNL5-L1Q-A111G by genetic engineering
9. Synthesis of γ-halogenated and long-chain β-hydroxy-α-amino acids and 2-amino-1,3-diols using threonine aldolases
10. Threonine aldolases—an emerging tool for organic synthesis
11. In situ proton-NMR analyses of Escherichia coli HB101 fermentations in (sup)1H(sub)2O and in D(sub)2O
12. Proton-nuclear magnetic resonance analyses of the substrate specificity of a beta-ketolase from Pseudomonas putida, acetopyruvate hydrolase
13. Chemoselective biotransformation of nitriles by Rhodococcus equi A4
14. Asymmetric biocatalytic hydrocyanation of pyrrole carboxaldehydes
15. Screening for hydroxynitrile lyases in plants
16. Novel Reductive Animation of Nitriles: An Efficient Route to 5-Hydroxypiperidone-Derived N, N-Acetals
17. Stereochemical course of two arene-cis-diol dehydrogenases specifically induced in Pseudomonas putida
18. 2-naptholate catabolic pathway in Burkholderia strain JT 1500
19. The first hydroxynitrile lyase catalysed cyanohydrin formation in ionic liquids
20. Hydroxynitrile lyase catalysed synthesis of heterocyclic ( R)- and ( S)-cyanohydrins
21. One-pot chemoenzymatic synthesis of protected cyanohydrins
22. Synthesis of all stereoisomeric carbapentofuranoses
23. Biocatalytic hydrolysis of cyanohydrins: an efficient approach to enantiopure α-hydroxy carboxylic acids
24. Novel access to chiral 1,1′-disubstituted ferrocene derivatives via double stereoselective cyanohydrin synthesis exploiting the hydroxynitrile lyase from Hevea brasiliensis
25. Chiral ferrocene cyanohydrin derivatives—access to novel intermolecularly linked and intramolecularly bridged ferrocene derivatives
26. Online NMR for monitoring biocatalysed reactions—the use of lipases in organic solvents
27. Oxidative biotransformations using oxygenases
28. The use of substrate engineering in biohydroxylation
29. Selectivity of the ( S)-oxynitrilase from Hevea brasiliensis towards α- and β-substituted aldehydes
30. On the selectivity of oxynitrilases towards α-oxygenated aldehydes
31. Biotransformation of 3-substituted methyl ( R, S)-4-cyanobutanoates with nitrile- and amide-converting biocatalysts
32. Chiral auxiliaries as docking/protecting groups: biohydroxylation of selected ketones with Beauveria bassiana ATCC 7159
33. Oxynitrilases for asymmetric C–C bond formation
34. The synthesis of chiral cyanohydrins by oxynitrilases
35. A Novel Stereoselective Access to Substituted l-2-Deoxypentono-1,4-lactones and l-2-Deoxypentoses
36. A Chemoenzymatic Access to d- and l-Sphingosines Employing Hydroxynitrile Lyases
37. Parameters influencing stability and activity of a S-hydroxynitrile lyase from Hevea brasiliensis in two-phase systems
38. α-Alkoxy-β-dicarbonylverbindungen durch Acylierung von Lithiumenolaten: Kurze Mitteilung
39. Prins-Reaktionen mit Arylaldehyden, 2. Mitt. Diene
40. Prins-reaktionen mit arylaldehyden, 1. Mitt.: Arylolefine
41. N-(2,6-Dihalobenzoyl)-N′-pyrimidinylharnstoffe
42. Substituierte 5-Hydroxypyrimidine und ihre O,O-Diethylphosphorsäure-, O,O-Diethylthiophosphorsäure-und N,N-Dimethylcarbamidsäureester
43. Reduktion 4-substituierter Acetophenone mittels Hefe: Kurze Mitteilung
44. Zur Reaktion von 1,3-Oxazolidinen mit Dicarbonsäureanhydriden
45. Prins-Reaktionen mit Arylaldehyden, 3. Mitt.: Beteiligung einer säurekatalysiertenCannizzaro-Reaktion an der Produktbildung
46. N-Arylsulfonyl-N′-pyrimidinylsubstituierte Chloralaminale
47. N-(Arylaminosulfonyl)benzamide: Kurze Mitteilung
48. Prins-Reaktionen mit Arylaldehyden, 5. Mitt.: Zur Umsetzung mit 2-Buten und mit Cyclohexen
49. Ein Modell zur Beschreibung der Lanthaniden-induzierten Verschiebungen bei zweizähnigen Liganden—1,3-Diole
50. Chemoenzymatic large-scale preparation of homochiral bicyclo[3.2.0]hept-2-en-6-one
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