Publications from research projects of the IRTG 2678 (chronological order).
19.
Bioinspired crowding directs supramolecular polymerisation,
N. Bäumer, E. Castellanos, B. Soberats, G. Fernández,
Nat. Commun. 2023, 14, 1084. [doi:10.1038/s41467-023-36540-x]
N. Bäumer, E. Castellanos, B. Soberats, G. Fernández,
Nat. Commun. 2023, 14, 1084. [doi:10.1038/s41467-023-36540-x]
18.
Enantioselective dearomatization reactions of heteroarenes by anion-binding organocatalysis,
M. Aleksiev, O. García Mancheño,
Chem. Commun. 2023, 59, accepted. [doi:10.1039/D2CC07101K]
M. Aleksiev, O. García Mancheño,
Chem. Commun. 2023, 59, accepted. [doi:10.1039/D2CC07101K]
17.
Metal-free photosensitized radical relay 1,4-carboimination across two distinct olefins,
G. Tan, F. Paulus, A. Petti, M.-A. Wiethoff, A. Lauer, C. G. Daniliuc, F. Glorius,
Chem. Sci. 2023, 14, 2447-2454. [doi:10.1039/D2SC06497A]
G. Tan, F. Paulus, A. Petti, M.-A. Wiethoff, A. Lauer, C. G. Daniliuc, F. Glorius,
Chem. Sci. 2023, 14, 2447-2454. [doi:10.1039/D2SC06497A]
16.
EnT-Mediated N–S Bond Homolysis of a Bifunctional Reagent Leading to Aliphatic Sulfonyl Fluorides,
J. E. Erchinger, R. Hoogesteger, R. Laskar, S. Dutta, C. Hümpel, D. Rana, C. G. Daniliuc, F. Glorius,
J. Am. Chem. Soc. 2023, 145, 2364–2374. [doi:10.1021/jacs.2c11295]
J. E. Erchinger, R. Hoogesteger, R. Laskar, S. Dutta, C. Hümpel, D. Rana, C. G. Daniliuc, F. Glorius,
J. Am. Chem. Soc. 2023, 145, 2364–2374. [doi:10.1021/jacs.2c11295]
15.
The subsystem quantum chemistry program Serenity,
N. Niemeyer, P. Eschenbach, M. Bensberg, J. Tölle, L. Hellmann, L. Lampe, A. Massolle, A. Rikus, D. Schnieders, J. P. Unsleber, J. Neugebauer,
WIREs Comput. Mol. Sci. 2022, e1647. [doi:10.1002/wcms.1647]
N. Niemeyer, P. Eschenbach, M. Bensberg, J. Tölle, L. Hellmann, L. Lampe, A. Massolle, A. Rikus, D. Schnieders, J. P. Unsleber, J. Neugebauer,
WIREs Comput. Mol. Sci. 2022, e1647. [doi:10.1002/wcms.1647]
14.
Impact of Hydrophobic/Hydrophilic Balance on Aggregation Pathways, Morphologies, and Excited-State Dynamics of Amphiphilic Diketopyrrolopyrrole Dyes in Aqueous Media,
N. Fukaya, S. Ogi, H. Sotome, K. J. Fujimoto, T. Yanai, N. Bäumer, G. Fernández, H. Miyasaka, S. Yamaguchi,
J. Am. Chem. Soc. 2022, 144, 22479-22492. [doi:10.1021/jacs.2c07299]
N. Fukaya, S. Ogi, H. Sotome, K. J. Fujimoto, T. Yanai, N. Bäumer, G. Fernández, H. Miyasaka, S. Yamaguchi,
J. Am. Chem. Soc. 2022, 144, 22479-22492. [doi:10.1021/jacs.2c07299]
13.
Highly Selective Radical Relay 1,4-Oxyimination of Two Electronically Differentiated Olefins ,
G. Tan, F. Paulus, A. Retería-Gómez, R. F. Lalisse, C. G. Daniliuc, O. Gutierrez, F. Glorius,
J. Am. Chem. Soc. 2022, 144, 21664-21673. [doi:10.1021/jacs.2c09244]
G. Tan, F. Paulus, A. Retería-Gómez, R. F. Lalisse, C. G. Daniliuc, O. Gutierrez, F. Glorius,
J. Am. Chem. Soc. 2022, 144, 21664-21673. [doi:10.1021/jacs.2c09244]
12.
Reliable Isotropic Electron-Paramagnetic-Resonance Hyperfine Coupling Constants from the Frozen-Density Embedding Quasi-Diabatization Approach,
P. Eschenbach, D. G. Artiukhin, J. Neugebauer,
J. Phys. Chem. A 2022, 157, 8358-5368. [doi:10.1021/acs.jpca.2c04959]
P. Eschenbach, D. G. Artiukhin, J. Neugebauer,
J. Phys. Chem. A 2022, 157, 8358-5368. [doi:10.1021/acs.jpca.2c04959]
11.
Subsystem density-functional theory: A reliable tool for spin-density based properties,
P. Eschenbach, J. Neugebauer,
J. Chem. Phys. 2022, 157, 130902. [doi:10.1063/5.0103091]
P. Eschenbach, J. Neugebauer,
J. Chem. Phys. 2022, 157, 130902. [doi:10.1063/5.0103091]
10.
Thermoreversible Polymorph Transitions in Supramolecular Polymers of Hydrogen-Bonded Squaramides,
S. Bujosa, A. Doncel-Giménez, N. Bäumer, G. Fernández, E. Ortí, A. Costa, C. Rotger, J. Aragó, B. Soberats,
Angew. Chem. Int. Ed. 2022, 61, e202213345. [doi:10.1002/anie.202213345]
S. Bujosa, A. Doncel-Giménez, N. Bäumer, G. Fernández, E. Ortí, A. Costa, C. Rotger, J. Aragó, B. Soberats,
Angew. Chem. Int. Ed. 2022, 61, e202213345. [doi:10.1002/anie.202213345]
9.
Chromium/Photoredox Dual Catalyzed Synthesis of α-Benzylic Alcohols, Isochromanones, 1,2-Oxy Alcohols and 1,2-Thio Alcohols,
S. Dutta, J. E. Erchinger, F. Schäfer, A. Das, C. G. Daniliuc, F. Glorius,
Angew. Chem. Int. Ed. 2022, 61, e202212136. [doi:10.1002/anie.202212136]
S. Dutta, J. E. Erchinger, F. Schäfer, A. Das, C. G. Daniliuc, F. Glorius,
Angew. Chem. Int. Ed. 2022, 61, e202212136. [doi:10.1002/anie.202212136]
8.
Oxy-Borylenes as Photoreductants: Synthesis and Application in Dehalogenation and Detosylation Reactions,
P. Lenz, R. Oshimizu, S. Klabunde, C. G. Daniliuc, C. Mück-Lichtenfeld, J. C. Tendyck, T. Mori, W. Uhl, M. R. Hansen, H. Eckert, S. Yamaguchi, A. Studer,
Angew. Chem. Int. Ed. 2022, 61, e202209391. [doi:10.1002/anie.202209391]
P. Lenz, R. Oshimizu, S. Klabunde, C. G. Daniliuc, C. Mück-Lichtenfeld, J. C. Tendyck, T. Mori, W. Uhl, M. R. Hansen, H. Eckert, S. Yamaguchi, A. Studer,
Angew. Chem. Int. Ed. 2022, 61, e202209391. [doi:10.1002/anie.202209391]
7.
Visible-Light Photocatalyzed peri-(3 + 2) Cycloadditions of Quinolines,
P. Bellotti, T. Rogge, F. Paulus, R. Laskar, N. Rendel, J. Ma, K. N. Houk, F. Glorius,
J. Am. Chem. Soc. 2022, 144, 15662-15671. [doi:10.1021/jacs.2c05687]
P. Bellotti, T. Rogge, F. Paulus, R. Laskar, N. Rendel, J. Ma, K. N. Houk, F. Glorius,
J. Am. Chem. Soc. 2022, 144, 15662-15671. [doi:10.1021/jacs.2c05687]
6.
Direct Access to Unnatural Cyclobutane α-Amino Acids through Visible Light Catalyzed [2+2]-Cycloaddition,
M. Stinglhamer, X. Yzeiri, T. Rohlfs, T. Brandhofer. C. G. Daniliuc, O. G. Mancheño,
ACS Org. Inorg. Au 2022, 2, 496-501. [doi:10.1021/acsorginorgau.2c00026]
M. Stinglhamer, X. Yzeiri, T. Rohlfs, T. Brandhofer. C. G. Daniliuc, O. G. Mancheño,
ACS Org. Inorg. Au 2022, 2, 496-501. [doi:10.1021/acsorginorgau.2c00026]
5.
Regio- and Enantioselective Intermolecular Aminofluorination of Alkenes via Iodine(I)/Iodine(III) Catalysis,
M. Schäfer, T. Stünkel, C. G. Daniliuc and R. Gilmour,
Angew. Chem. Int. Ed. 2022, 61, e202205508. [doi:10.1002/anie.202205508]
M. Schäfer, T. Stünkel, C. G. Daniliuc and R. Gilmour,
Angew. Chem. Int. Ed. 2022, 61, e202205508. [doi:10.1002/anie.202205508]
4.
A negative-solvatochromic fluorescent probe for visualizing intracellular distributions of fatty acid metabolites,
K. Kajiwara, H. Osaki, S. Greßies, K. Kuwata, J. H. Kim, T. Gensch, Y. Sato, F. Glorius, S. Yamaguchi, M. Taki,
Nat. Commun. 2022, 13, 1370. [doi:10.1038/s41467-022-29086-x]
K. Kajiwara, H. Osaki, S. Greßies, K. Kuwata, J. H. Kim, T. Gensch, Y. Sato, F. Glorius, S. Yamaguchi, M. Taki,
Nat. Commun. 2022, 13, 1370. [doi:10.1038/s41467-022-29086-x]
3.
Expanding the Scope of MetastableSpecies in Hydrogen Bonding-Directed SupramolecularPolymerization,
J. Matern, Z. Fernández, N. Bäumer, G. Fernández,
Angew. Chem. Int. Ed. 2022, 61, e202203783. [doi:10.1002/anie.202203783]
J. Matern, Z. Fernández, N. Bäumer, G. Fernández,
Angew. Chem. Int. Ed. 2022, 61, e202203783. [doi:10.1002/anie.202203783]
2.
Anti-cooperative Self-Assembly with Maintained Emission Regulated by Conformational and Steric Effects,
I. Helmers, M. S. Hossain, N. Bäumer, P. Wesarg, B. Soberats, L. S. Shimizu, G. Fernández,
Angew. Chem. Int. Ed. 2022, 61, e202200390. [doi:10.1002/anie.202200390]
I. Helmers, M. S. Hossain, N. Bäumer, P. Wesarg, B. Soberats, L. S. Shimizu, G. Fernández,
Angew. Chem. Int. Ed. 2022, 61, e202200390. [doi:10.1002/anie.202200390]
1.
Regio- and Stereoselective 1,2-Carboboration of Ynamides with Aryldichloroboranes,
C. You, M. Sakai, C. G. Daniliuc, K. Bergander, S. Yamaguchi, A. Studer,
Angew. Chem. Int. Ed. 2021, 60, 21697-21701. [doi:10.1002/anie.202107647]
C. You, M. Sakai, C. G. Daniliuc, K. Bergander, S. Yamaguchi, A. Studer,
Angew. Chem. Int. Ed. 2021, 60, 21697-21701. [doi:10.1002/anie.202107647]