17. Photoswitchable Nitrogen Superbases: Using Light for Reversible Carbon Dioxide Capture

L. F. B. Wilm, M. Das, D. Janssen-Müller, C. Mück-Lichtenfeld, F. Glorius, F. Dielmann, Angew. Chem. Int. Ed. 2021, early view DOI

16.     Ni-Catalyzed Carboxylation of Aziridines en Route to β-Amino Acids

J. Davies, D. Janssen-Müller, D. P. Zimin, D. P., C. S. Day, T. Yanagi, J. Elfert, R. Martin J. Am. Chem. Soc. 2021, 143, 4949–4954. DOI

15.     Remote sp2 C–H Carboxylation via Catalytic 1,4-Ni Migration with CO2

M. Börjesson, D. Janssen-Müller, B. Sahoo, Y. Duan, X. Wang, and R. Martin J. Am. Chem. Soc. 2020, 142, 16234–16239. DOI

14.    Transition‐Metal‐Like Catalysis with a Main‐Group Element: Bismuth‐Catalyzed C−F Coupling of Aryl Boronic Esters

D. Janssen-Müller, M. Oestreich, Angew. Chem. Int. Ed. 2020, 59, 8328-8330. DOI

13.    Tackling Remote sp3 C−H Functionalization via Ni‐Catalyzed “chain‐walking” Reactions

D. Janssen‐Müller, B. Sahoo, S.‐Z. Sun, R. Martin, Israel J. Chem. 2020, 60, 195-206. DOI

12.    Cyclic (Aryl)(Amido)-Carbenes: NHCs with Triplet‐like Reactivity

P. R. Sultane, G. Ahumada, D. Janssen‐Müller, C. W. Bielawski, Angew. Chem. Int. Ed. 2019, 58, 16320–16325. DOI

11.    Privileged Chiral N-Heterocyclic Carbene Ligands for Asymmetric Transition-Metal Catalysis

D. Janssen-Müller, C. Schlepphorst, F. Glorius, Chem. Soc. Rev. 2017, 46, 4845-4854. DOI

10.    NHC-Organocatalyzed CAr–O Bond Cleavage: Mild access to 2-Hydroxybenzophenones

D. Janssen-Müller, S. Singha, F. Lied, K. Gottschalk, F. Glorius, Angew. Chem. Int. Ed. 2017, 56, 6276-6279. DOI
Highlighted in Synfacts 2017, 13, 0651.

9.    Mechanistic Studies on a Cooperative NHC Organocatalysis/Palladium Catalysis System: Uncovering Significant Lessons for Mixed Chiral Pd(NHC)(PR3) Catalyst Design

C. Guo, D. Janssen-Müller, M. Fleige, A. Lerchen, C. G. Daniliuc, F. Glorius, J. Am. Chem. Soc. 2017, 139, 4443-4451. DOI

8.    Synthesis of the homochiral metal-organic framework DUT-129 based on a chiral dicarboxylate linker with 6 stereocenters

C. Kutzscher, D. Janssen-Müller, A. Notzon, U. Stoeck, V. Bon, I. Senkovska, S. Kaskel, F. Glorius, CrystEngComm. 2017, 19, 2494-2499. DOI

7.    Cooperative N-Heterocyclic Carbene/Palladium-Catalyzed Enantioselective Umpolung Annulations

C. Guo, M. Fleige, D. Janssen-Müller, C. G. Daniliuc, F. Glorius, J. Am. Chem. Soc. 2016, 138, 7840 7843. DOI

6.    Annulation of o-Quinodimethanes (o-QDM) through NHC-Catalysis for the Synthesis of 1-Isochromanones

D. Janssen-Müller, S. Singha, T. Olyschläger, C. G. Daniliuc, F. Glorius, Org. Lett. 2016, 18, 4444-4447. DOI
Highlighted in Synfacts 2016, 12, 1125.

5.    NHC-Catalyzed Enantioselective Dearomatizing Hydroacylation of Benzofurans and Benzothiophenes for the Synthesis of Spirocycles

D. Janssen-Müller, M. Fleige, D. Schlüns, M. Wollenburg, C. G. Daniliuc, J. Neugebauer, F. Glorius, ACS Catal. 2016, 6, 5735-5739. DOI

4.    Enantioselective Intramolecular Hydroacylation of Unactivated Alkenes: An NHC-Catalyzed Robust and Versatile Formation of Cyclic Chiral Ketones

D. Janssen-Müller, M. Schedler, M. Fleige, C. G. Daniliuc, F. Glorius, Angew. Chem. Int. Ed. 2015, 54, 12492-12496. DOI
    Highlighted in Synfacts 2015, 11, 659 as Synfact of the month.

3.     Switchable selectivity in an NHC-catalysed dearomatizing annulation reaction

C. Guo, M. Fleige, D. Janssen-Müller, C. G. Daniliuc, F. Glorius, Nature Chem. 2015, 7, 842-847. DOI

2.     Functional group tolerance in BTB-based metal–organic frameworks (BTB – benzene-1,3,5-tribenzoate)

S. Helten, B. Sahoo, P. Müller, D. Janssen-Müller, N. Klein, R. Grünker, V. Bon, F. Glorius, S. Kaskel, I. Senkovska, , Microporous Mesoporous Mater. 2015, 216, 42-50. DOI

1.     Systematic detection of hidden complexities in the unfolding mechanism of a cytosine-rich DNA strand

J. Smiatek, D. Janssen-Müller, R. Friedrich, A. Heuer, Physica A 2014, 394, 136-144. DOI