Artículos con órdenes de acceso público - Peter R. SchreinerMás información
No disponibles en ningún lugar: 125
(Thio) urea organocatalysis—What can be learnt from anion recognition?
Z Zhang, PR Schreiner
Chemical Society Reviews 38 (4), 1187-1198, 2009
Órdenes: German Research Foundation
London dispersion in molecular chemistry—reconsidering steric effects
JP Wagner, PR Schreiner
Angewandte Chemie International Edition 54 (42), 12274-12296, 2015
Órdenes: German Research Foundation
Organocatalytic Enantioselective Acyl Transfer onto Racemic as well as meso Alcohols, Amines, and Thiols
CE Müller, PR Schreiner
Angewandte Chemie International Edition 50 (27), 6012-6042, 2011
Órdenes: German Research Foundation
(Thio) urea organocatalyst equilibrium acidities in DMSO
G Jakab, C Tancon, Z Zhang, KM Lippert, PR Schreiner
Organic letters 14 (7), 1724-1727, 2012
Órdenes: German Research Foundation
Steric crowding can stabilize a labile molecule: solving the hexaphenylethane riddle
S Grimme, PR Schreiner
Angewandte Chemie International Edition 50 (52), 12639-12642, 2011
Órdenes: German Research Foundation
Acid-free, organocatalytic acetalization
M Kotke, PR Schreiner
Tetrahedron 62 (2-3), 434-439, 2006
Órdenes: German Research Foundation
Stable alkanes containing very long carbon–carbon bonds
AA Fokin, LV Chernish, PA Gunchenko, EY Tikhonchuk, H Hausmann, ...
Journal of the American Chemical Society 134 (33), 13641-13650, 2012
Órdenes: German Research Foundation
Diamondoids: functionalization and subsequent applications of perfectly defined molecular cage hydrocarbons
MA Gunawan, JC Hierso, D Poinsot, AA Fokin, NA Fokina, BA Tkachenko, ...
New Journal of Chemistry 38 (1), 28-41, 2014
Órdenes: German Research Foundation
Tunneling control of chemical reactions: the third reactivity paradigm
PR Schreiner
Journal of the American Chemical Society 139 (43), 15276-15283, 2017
Órdenes: German Research Foundation
London’sche Dispersionswechselwirkungen in der Molekülchemie–eine Neubetrachtung sterischer Effekte
JP Wagner, PR Schreiner
Angewandte Chemie 127 (42), 12446-12471, 2015
Órdenes: German Research Foundation
Hydrogen‐bonding thiourea organocatalysts: the privileged 3, 5‐bis (trifluoromethyl) phenyl group
KM Lippert, K Hof, D Gerbig, D Ley, H Hausmann, S Guenther, ...
European Journal of Organic Chemistry 2012 (30), 5919-5927, 2012
Órdenes: German Research Foundation
London dispersion enables the shortest intermolecular hydrocarbon H··· H contact
S Rösel, H Quanz, C Logemann, J Becker, E Mossou, ...
Journal of the American Chemical Society 139 (22), 7428-7431, 2017
Órdenes: German Research Foundation
Cooperative brønsted acid-type organocatalysis: alcoholysis of styrene oxides
T Weil, M Kotke, CM Kleiner, PR Schreiner
Organic Letters 10 (8), 1513-1516, 2008
Órdenes: German Research Foundation
Functionalized nanodiamonds: Triamantane and [121] tetramantane
PR Schreiner, NA Fokina, BA Tkachenko, H Hausmann, M Serafin, ...
The Journal of Organic Chemistry 71 (18), 6709-6720, 2006
Órdenes: German Research Foundation
Hydrophobic amplification of noncovalent organocatalysis
CM Kleiner, PR Schreiner
Chemical communications, 4315-4317, 2006
Órdenes: German Research Foundation
Enantioselective Kinetic Resolution of trans‐Cycloalkane‐1,2‐diols
CE Müller, L Wanka, K Jewell, PR Schreiner
Angewandte Chemie International Edition 47 (33), 6180-6183, 2008
Órdenes: German Research Foundation
γ‐Aminoadamantanecarboxylic Acids Through Direct C–H Bond Amidations
L Wanka, C Cabrele, M Vanejews, PR Schreiner
European journal of organic chemistry 2007 (9), 1474-1490, 2007
Órdenes: German Research Foundation
A silicon–carbonyl complex stable at room temperature
C Ganesamoorthy, J Schoening, C Wölper, L Song, PR Schreiner, ...
Nature Chemistry 12 (7), 608-614, 2020
Órdenes: German Research Foundation
London dispersion decisively contributes to the thermodynamic stability of bulky NHC-coordinated main group compounds
JP Wagner, PR Schreiner
Journal of Chemical Theory and Computation 12 (1), 231-237, 2016
Órdenes: German Research Foundation
Organokatalytischer, enantioselektiver Acyltransfer auf racemische sowie meso‐Alkohole,‐Amine und‐Thiole
CE Müller, PR Schreiner
Angewandte Chemie 123 (27), 6136-6167, 2011
Órdenes: German Research Foundation
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