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1.
Hemmler, D. et al.: Simulated sunlight sectively modifies maillard reaction products in a wide array of chemical reactions. Chem. Eur. J. 25, 13208-13217 (2019)
2.
Raltchev, K. ; Pipercevic, J. & Hagn, F.: Production and structural analysis of membrane-anchored proteins in phospholipid nanodiscs. Chem. Eur. J. 24, 5493-5499 (2018)
3.
Schwarzenböck, C.* et al.: Fluorescent polyvinylphosphonate bioconjugates for selective cellular delivery. Chem. Eur. J. 24, 2584-2587 (2018)
4.
Sanchez-Rico, C. ; VoithvonVoithenberg, L.* ; Warner, L. ; Lamb, D.C.* & Sattler, M.: Effects of fluorophore attachment on protein conformation and dynamics studied by spFRET and NMR spectroscopy. Chem. Eur. J. 23, 14267-14277 (2017)
5.
Dallmann, A. et al.: Site-specific isotope-labeling of inosine phosphoramidites and NMR analysis of an inosine-containing RNA duplex. Chem. Eur. J. 22, 15350-15359 (2016)
6.
Börjesson, K.* et al.: Exploring the potential of fulvalene dimetals as platforms for molecular solar thermal energy storage: Computations, syntheses, structures, kinetics, and catalysis. Chem. Eur. J. 20, 15587-15604 (2014)
7.
Kadam, R.U.* et al.: Structure-based optimization of the terminal tripeptide in glycopeptide dendrimer inhibitors of Pseudomonas aeruginosa biofilms targeting LecA. Chem. Eur. J. 19, 17054-17063 (2013)
8.
Boutegrabet, L. et al.: Attachment of chloride anion to sugars: Mechanistic investigation and discovery of a new dopant for efficient sugar ionization/detection in mass spectrometers. Chem. Eur. J. 18, 13059-13067 (2012)
9.
Gougeon, R.D.* et al.: Expressing forest origins in the chemical composition of cooperage oak woods and corresponding wines by using FTICR-MS. Chem. Eur. J. 15, 600-611 (2009)
10.
Eissen, M.* & Lenoir, D.: Electrophilic bromination of alkenes: Environmental, health and safety aspects of new alternative methods. Chem. Eur. J. 14, 9830-9841 (2008)
11.
Jäger, R.* et al.: Selective adsorption of polychlorinated dibenzo-p-dioxins and dibenzofurans by the Zeosils UTD-1, SSZ-24 and ITQ-4. Chem. Eur. J. 10, 247-256 (2004)
12.
Lenoir, D. & Chiappe, C.*: What is the nature of the first-formed intermediates in the electrophilic halogenation of alkenes, alkynes and allenes? Chem. Eur. J. 9, 1037-1044 (2003)
13.
Lalah, J.O.* et al.: Regioselective Synthesis of a Branched Isomer of Nonylphenol, 4-(3',6'-Dimethyl-3'-heptyl)phenol and Determination of its Important Environmental Properties. Chem. Eur. J. 7, 4790-4795 (2001)
14.
Bianchini, R.* ; Chiappe, C.* ; Lenoir, D. & Goldberg, N.*: Spectroscopic and theoretical investigations of electrophilic bromination reactions of alkynes : The first evidence for complexes as reaction intermediates. Chem. Eur. J. 5, 1570-1580 (1999)