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Prof. Dr. Julia Rehbein
Prof. Dr. Julia Rehbein
Prof. of Chemistry, UR Germany
Verified email at ur.de - Homepage
Title
Cited by
Cited by
Year
Do we fully understand what controls chemical selectivity?
J Rehbein, BK Carpenter
Physical Chemistry Chemical Physics 13 (47), 20906-20922, 2011
1862011
Visible‐Light‐Accelerated Copper (II)‐Catalyzed Regio‐and Chemoselective Oxo‐Azidation of Vinyl Arenes
A Hossain, A Vidyasagar, C Eichinger, C Lankes, J Phan, J Rehbein, ...
Angewandte Chemie International Edition 57 (27), 8288-8292, 2018
1382018
Enantioselective oxidative rearrangements with chiral hypervalent iodine reagents
M Brown, R Kumar, J Rehbein, T Wirth
Chemistry–A European Journal 22 (12), 4030-4035, 2016
1122016
NHC-catalysed benzoin condensation–is it all down to the Breslow intermediate?
J Rehbein, SM Ruser, J Phan
Chemical Science 6 (10), 6013-6018, 2015
962015
Hole-mediated photoredox catalysis: tris (p-substituted) biarylaminium radical cations as tunable, precomplexing and potent photooxidants
S Wu, J Žurauskas, M Domański, PS Hitzfeld, V Butera, DJ Scott, ...
Organic Chemistry Frontiers 8 (6), 1132-1142, 2021
832021
Facile oxidative rearrangements using hypervalent iodine reagents
FV Singh, J Rehbein, T Wirth
ChemistryOpen 1 (6), 245-250, 2012
832012
Organocatalytic claisen rearrangement: theory and experiment
M Kirsten, J Rehbein, M Hiersemann, T Strassner
The Journal of Organic Chemistry 72 (11), 4001-4011, 2007
782007
Claisen rearrangement of aliphatic allyl vinyl ethers from 1912 to 2012: 100 years of electrophilic catalysis
J Rehbein, M Hiersemann
Synthesis 45 (09), 1121-1159, 2013
722013
Mechanistic and synthetic investigations on the dual selenium-π-acid/photoredox catalysis in the context of the aerobic dehydrogenative lactonization of alkenoic acids
S Ortgies, R Rieger, K Rode, K Koszinowski, J Kind, CM Thiele, ...
ACS Catalysis 7 (11), 7578-7586, 2017
632017
Gosteli− Claisen Rearrangement: Substrate Synthesis, Simple Diastereoselectivity, and Kinetic Studies
J Rehbein, S Leick, M Hiersemann
The Journal of Organic Chemistry 74 (4), 1531-1540, 2009
592009
Enantioselective electrochemical lactonization using chiral iodoarenes as mediators
WC Gao, ZY Xiong, S Pirhaghani, T Wirth
Synthesis 51 (01), 276-284, 2019
572019
Fluorine as a traceless directing group for the regiodivergent synthesis of indoles and tryptophans
A Andries-Ulmer, C Brunner, J Rehbein, T Gulder
Journal of the American Chemical Society 140 (40), 13034-13041, 2018
562018
Total Synthesis of Natural and Non-Natural Δ5,6Δ12,13-Jatrophane Diterpenes and Their Evaluation as MDR Modulators
C Schnabel, K Sterz, H Müller, J Rehbein, M Wiese, M Hiersemann
The Journal of Organic Chemistry 76 (2), 512-522, 2011
562011
Gosteli− Claisen Rearrangement of Propargyl Vinyl Ethers: Cascading Molecular Rearrangements
A Gille, J Rehbein, M Hiersemann
Organic Letters 13 (8), 2122-2125, 2011
402011
Development of an Alkyne Analogue of the de Mayo Reaction: Synthesis of Medium‐Sized Carbacycles and Cyclohepta[b]indoles
D Tymann, DC Tymann, U Bednarzick, L Iovkova‐Berends, J Rehbein, ...
Angewandte Chemie International Edition 57 (47), 15553-15557, 2018
382018
Integration of catalysis and analysis is the key: rapid and precise investigation of the catalytic asymmetric Gosteli–Claisen rearrangement
J Troendlin, J Rehbein, M Hiersemann, O Trapp
Journal of the American Chemical Society 133 (41), 16444-16450, 2011
342011
Copper (II)-photocatalyzed decarboxylative oxygenation of carboxylic acids
A Reichle, H Sterzel, P Kreitmeier, R Fayad, FN Castellano, J Rehbein, ...
Chemical Communications 58 (28), 4456-4459, 2022
332022
Chemistry in motion—off the MEP
J Rehbein, B Wulff
Tetrahedron letters 56 (50), 6931-6943, 2015
312015
Gosteli− Claisen rearrangement: DFT study of substituent− rate effects
J Rehbein, M Hiersemann
The Journal of Organic Chemistry 74 (11), 4336-4342, 2009
312009
Ir(ppy)3-Catalyzed, Visible-Light-Mediated Reaction of α-Chloro Cinnamates with Enol Acetates: An Apparent Halogen Paradox
T Föll, J Rehbein, O Reiser
Organic letters 20 (18), 5794-5798, 2018
292018
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