chiralnr.html

Referenzen für Dr.Maisch Reprosil Chiral HPLC-Säulen

siehe auch Chirapedia mit Substanzindex

- Linoleate 9R-dioxygenase and allene oxide synthase activities of Aspergillus terreus. F. Jernerén, Archives of Biochemistry and Biophysics, on-line, DOI: 10.1016/j.abb.2009.12.022v (Reprosil 100 Chiral-NR, 5 µm 250 x 2 mm; Reprosil Chiral-AM, 5 µm 250 x 2 mm)

- Novel heterocyclic compounds. J.M. Adam, Patent, Nr. 20100022518 (2010). (Reprosil 100 Chiral-NR, 8 µm)

- Leucine/valine residues direct oxygenation of linoleic acid by (10R)- and (8R)-dioxygenases. U. Garscha, Journal of Biological Chemistry, 284 (2009) 13755-13765. (Reprosil 100 Chiral-NR, 8 µm, 250 x 2 mm; Reprosil Chiral-AM, 10 µm, 150 x 2 mm)

- alpha-Substituted norstatines as the transition-state mimic in inhibitors of multiple digestive vacuole malaria aspartic proteases. K.M.Orrling, Bioorganic & Medical Chemistry, 17 (2009) 5933-5949. (Reprosil 100 Chiral-NRR, 8 µm, 250 x 4.6 mm, 250 x 20 mm)

- Synthesis and biological evaluation of pretubulysin and derivatives. A. Ulrich, European Journal of Organic Chemistry, 36 (2009) 6367-6378. (ReproSil 100 Chiral-NR, 8 µm)

- Mass spectrometric analysis of oxylipins. Application to cytochrome P450-dependent metabolism. T. Nilsson, Dissertation, Uppsala University, 2009. (ReproSil 100 Chiral-NR und -NR-R, 8 µm, 250 x 4 mm)

- Synthesis of chlamydocin by chelate-Claisen rearrangement. Ch. Quirin, European Journal of Organic Chemistry, 3 (2009) 371-377. (Reprosil 100 Chiral-NR, 8 µm, 250 x 4.6 mm)

- Synthese unnatürlicher Aminosäure-Derivate via Esterenolat-Claisen-Umlagerung und deren Anwendung in der Naturstoffsynthese. Ch. Quirin, Dissertation, Universität Saarbrücken, 2008. (Reprosil 100 Chiral-NR, 8 µm, 250 x 4.6 mm)

Reprosil Chiral-AM

- Secretion of two novel enzymes, manganese 9S-lipoxygenase and epoxy alcohol synthase, by the rice pathogen Magnaporthe salvinii. A. Wennman, Journal of Lipid Research, 54 (2013) 762-775. (Reprosil Chiral-AM, 5 um, 250 x 2 mm)

- Catalytic Convergence of Manganese and Iron Lipoxygenases by Replacement of a Single Amino Acid. A. Wennman, The Journal of Biological Chemistry, 287 (2012) 31757-31765. (Reprosil 100 Chiral-NR, 8 μm, 250 x 2 mm; Reprosil Chiral-AM, 5 μm, 250 x 2 mm) - Supplemental Data

- Idenification of putative residues involved in the accessibility of the substrate-binding site of lipogenase by site-directed mutagenesis studies. C. Palmieri-Thiers, Archives of Biochemistry and Biophysics, 509 (2011) 82-89. (Reprosil Chiral-AM, 10 μm, 250 x 2 mm)

- LC-MS/MS analysis of epoxyalcohols and epoxides of arachidonic acid and their oxygenation by recombinant CYP4F8 and CYP4F22. T. Nilsson, Archives of Biochemistry and Biophysics, 494 (2010) 64-71. (Reprosil Chiral-AM, 5 µm, 250 x 2 mm; Reprosil Chiral-NR, 8 µm, 250 x 4 mm)

- Peptides as catalysts for asymmetric 1,4-addition reactions of aldehydes to nitroolefins. M. Wiesner, Dissertation, Universität Basel, 2009. (Reprosil Chiral AM, 250 mm x 4.6 mm)

- Linoleate 9R-dioxygenase and allene oxide synthase activities of Aspergillus terreus. F. Jernerén, Archives of Biochemistry and Biophysics, on-line, DOI: 10.1016/j.abb.2009.12.022v (Reprosil Chiral-AM, 5 µm 250 x 2 mm und Reprosil Chiral-NR, 5 µm 250 x 2 mm)

- A lipoxygenase with dual positional specificity is expressed in olives (Olea europaea L.) during ripening. C. Palmieri-Thiers, Biochimica et Biophysica acta, 1791 (2009) 339-346. (Reprosil Chiral-AM, 10 µm, 250 x 2 mm)

- Leucine/valine residues direct oxygenation of linoleic acid by (10R)- and (8R)-dioxygenases. U. Garscha, Journal of Biological Chemistry, 284 (2009) 13755-13765. (Reprosil Chiral-AM, 10 µm, 250 x 2 mm; ReproSil Chiral-NR, 8 µm, 250 x 2 mm)

- Research review. A.J. Ram, Pharma Express, 16-31. March 2009. (ReproSil Chiral-CA, 5 µm, 250 x 2 mm)

- Applications of LC-MS to quantitation and evaluation of the environmental fate of chiral drugs and their metabolites. S. Pérez,
Trends in Analytical Chemistry,
27 (2008) 836-846. (Reprosil Chiral-CA)

- Enantioselective quantification of omeprazole and its main metabolites in human serum by chiral HPLC–atmospheric pressure photoionization tandem mass spectrometry. J. Martens-Lobenhoffer, Journal of Chromatography B, 857 (2007) 301-307. (Reprosil Chiral-CA, 5 µm, 250 x 2 mm)

Referenzen für Dr.Maisch Reprosil Chiral HPLC-Säulen

- Ni(II)-catalyzed enantioselective Nazarov cyclizations. I. Walz, Chemical Communications, (2008) 4315-4317. (Reprosil 100 Chiral-NR, 8 µm, 250 x 20 mm)