5 article(s) from Flitsch, Sabine L
Library generation of P450cam[Tyr96Phe]-RhFRed. Active site of the P450cam-RhFRed variant Tyr96Phe ...
Jump to Figure 1
Radar plots illustrating the substrate acceptance of P450cam-RhFRed variants from library I. Colour...
Jump to Figure 2
Yields of alcohols (R,S)-9-11 (grey bars) and ketone products 13–15 (blue bars) in sub-pools of lib...
Jump to Figure 3
Beilstein J. Org. Chem. 2015, 11, 1713–1720, doi:10.3762/bjoc.11.186
Carbohydrate arrays on polystyrene slides can be obtained by noncovalent immobilisation of tritylat...
Synthesis of the tritylated compounds 3 , 5 and 7: (a) dichloromethane, 2.5 h, rt, 98%, (b) HBTU/DI...
Jump to Scheme 1
Comparison of the polystyrene and glass surfaces with and without aluminium backing by matrix-free ...
The Man–Trt compound 5 forms the disulfide 8 during UV ionisation in MALDI-TOF MS analysis.
Jump to Scheme 2
Limit-of-detection analysis of 5 on aluminium-backed glass and polystyrene slides. Both systems sho...
Comparison of MALDI-TOF MS spectra on the aluminium-backed polystyrene and glass slides after washi...
Jump to Figure 4
Photo of the aluminium strip on the back of the polystyrene support.
Jump to Figure 5
Beilstein J. Org. Chem. 2012, 8, 753–762, doi:10.3762/bjoc.8.86
Regioselective hydroxylation of Cbz-piperidine by Rhodococcus rhodochrous resting cells.
Results from the incubation of THP ether derivatives with Rhodococcus rhodochrous showing the isola...
Influence of substrate structure and linker length on the regioselectivity of hydroxylation.
Jump to Scheme 3
Regioselective hydroxylation following incubation of THF ether derivatives with Rhodococcus rhodoch...
Jump to Scheme 4
Beilstein J. Org. Chem. 2012, 8, 496–500, doi:10.3762/bjoc.8.56
Oxidation reactions with P450cam-RhFRed mutants.
Whole cell biotransformation of diphenylmethane to 4-hydroxydiphenylmethane with P450cam(Y96A)-RhFR...
Beilstein J. Org. Chem. 2011, 7, 1494–1498, doi:10.3762/bjoc.7.173
Aminoethyl glycosides (1–9) which were synthesised in this study.
General reaction scheme for generation of aminoethyl glycosides. X = OAc, Br or Cl.
Beilstein J. Org. Chem. 2010, 6, 699–703, doi:10.3762/bjoc.6.81
Subscribe to our Latest Articles RSS Feed.
Register and get informed about new articles.
Follow the Beilstein-Institut