Publikationen der NMR-Abteilung

Niklas, T.; Schulze, P.; Farès, C.: Cromolyn/gelatin mixtures as aqueous alignment media and utilization of their mechanical stability for a layering technique. Magnetic Resonance in Chemistry 56 (12), S. 1176 - 1182 (2018)

Heinrich, M.; Murphy, J. J.; Ilg, M. K.; Letort, A.; Flasz, J.; Philipps, P.; Fürstner, A.: Total Synthesis of Putative Chagosensine. Angewandte Chemie International Edition 57 (41), S. 13575 - 13581 (2018)

Anderl, F.; Größl, S.; Wirtz, C.; Fürstner, A.: Total Synthesis of Belizentrin Methyl Ester: Report on a Likely Conquest. Angewandte Chemie International Edition 57 (33), S. 10712 - 10717 (2018)

Pupier, M.; Nuzillard, J.-M.; Wist, J.; Schlörer, N. E.; Kuhn, S.; Erdelyi, M.; Steinbeck, C.; Williams, A. J.; Butts, C.; Claridge, T. D. W. et al.; Mikhova, B.; Robien, W.; Dashti, H.; Eghbalnia, H. R.; Farès, C.; Adam, C.; Kessler, P.; Moriaud, F.; Elyashberg, M.; Argyropoulos, D.; Pérez, M.; Giraudeau, P.; Gil, R. R.; Trevorrow, P.; Jeannerat, D.: NMReDATA, a standard to report the NMR assignment and parameters of organic compounds. Magnetic Resonance in Chemistry 56 (8), S. 703 - 715 (2018)

Höfler, D.; Goddard, R.; Lingnau, J. B.; Nöthling, N.; List, B.: A Purely Organic Tricarbanion. Angewandte Chemie International Edition 57 (27), S. 8326 - 8329 (2018)

Sommer, C.; Rumpel, S.; Roy, S.; Farès, C.; Artero, V.; Fontecave, M.; Reijerse, E.; Lubitz, W.: Spectroscopic investigations of a semi-synthetic [FeFe] hydrogenase with propane di-selenol as bridging ligand in the binuclear subsite: comparison to the wild type and propane di-thiol variants. Journal of Biological Inorganic Chemistry 23 (3), S. 481 - 491 (2018)

Acevedo-Rocha, C. G.; Gamble, C. G.; Lonsdale, R.; Li, A.; Nett, N.; Hoebenreich, S.; Lingnau, J. B.; Wirtz, C.; Fares, C.; Hinrichs, H. et al.; Deege, A.; Mulholland, A. J.; Nov, Y.; Leys, D.; McLean, K. J.; Munro, A. W.; Reetz, M. T.: P450-Catalyzed Regio- and Diastereoselective Steroid Hydroxylation: Efficient Directed Evolution Enabled by Mutability Landscaping. ACS Catalysis 8 (4), S. 3395 - 3410 (2018)

Wiegand, K.; Winkler, M.; Rumpel, S.; Kannchen, D.; Rexroth, S.; Hase, T.; Farès, C.; Happe, T.; Lubitz, W.; Rögner, M.: Rational redesign of the ferredoxin-NADP⁺-oxido-reductase/ferredoxin-interaction for photosynthesis-dependent H₂-production. Biochimica et Biophysica Acta, Bioenergetics 1859 (4), S. 253 - 262 (2018)

Tsuji, N.; Kennemur, J. L.; Buyck, T.; Lee, S.; Prévost, S.; Kaib, P. S. J.; Bykov, D.; Farès, C.; List, B.: Activation of olefins via asymmetric Brønsted acid catalysis. Science 359 (6383), S. 1501 - 1505 (2018)

Rumpel, S.; Sommer, C.; Reijerse, E.; Farès, C.; Lubitz, W.: Direct Detection of the Terminal Hydride Intermediate in [FeFe] Hydrogenase by NMR Spectroscopy. Journal of the American Chemical Society 140 (11), S. 3863 - 3866 (2018)

Guthertz, A.; Leutzsch, M.; Wolf, L. M.; Gupta, P.; Rummelt, S. M.; Goddard, R.; Farès, C.; Thiel, W.; Fürstner, A.: Half-​Sandwich Ruthenium Carbene Complexes Link trans-​Hydrogenation and gem-​Hydrogenation of Internal Alkynes. Journal of the American Chemical Society 140 (8), S. 3156 - 3169 (2018)

Gatzenmeier, T.; Kaib, P. S. J.; Lingnau, J. B.; Goddard, R.; List, B.: The Catalytic Asymmetric Mukaiyama–Michael Reaction of Silyl Ketene Acetals with α,β-Unsaturated Methyl Esters. Angewandte Chemie International Edition 57 (9), S. 2464 - 2468 (2018)

Tindall, D. J.; Werlé, C.; Goddard, R.; Philipps, P.; Farès, C.; Fürstner, A.: Structure and Reactivity of Half-Sandwich Rh(+3) and Ir(+3) Carbene Complexes. Catalytic Metathesis of Azobenzene Derivatives. Journal of the American Chemical Society 140 (5), S. 1884 - 1893 (2018)

Rumpel, S.; Ravera, E.; Sommer, C.; Reijerse, E.; Farès, C.; Luchinat, C.; Lubitz, W.: ¹H NMR Spectroscopy of [FeFe] Hydrogenase: Insight into the Electronic Structure of the Active Site. Journal of the American Chemical Society 140 (1), S. 131 - 134 (2018)

Kwon, Y.; Schulthoff, S.; Dao, Q. M.; Wirtz, C.; Fürstner, A.: Total Synthesis of Disciformycin A and B: Unusually Exigent Targets of Biological Significance. Chemistry – A European Journal 24 (1), S. 109 - 114 (2018)