Go to JKU Homepage
Institute of Catalysis
What's that?

Institutes, schools, other departments, and programs create their own web content and menus.

To help you better navigate the site, see here where you are at the moment.

Marko Hapke - Research Results.

 

59.

“Cyclotrimerization Approach to Symmetric [9]-Helical Indenofluorenes: Diverting Cyclization Pathways”

T. Cadart, T. Gläsel, I. Císařová, R. Gyepes, M. Hapke, M. Kotora

Chem. Eur. J. 2023, 29, e202301491

Link: https://doi.org/10.1002/chem.202301491, opens an external URL in a new window

Grafik 59

58.

“Cobalt and Iron Metallates as Catalysts for Cyclization Reactions of Triynes: [2+2+2] Cycloaddition vs. Garratt-Braverman Reaction”

B. Baumann, H. Lange, F. Seeberger, P. Büschelberger, R. Wolf, M. Hapke

Mol. Catal, opens an external URL in a new window. 2023, 550, 113482

Link: https://doi.org/10.1016/j.mcat.2023.113482, opens an external URL in a new window

Grafik 58

57.

“Atroposelective Ir-catalyzed C-H borylation of phthalazine heterobiaryls”

P. Stehrer, A. Spannenberg, M. Hapke

J. Org. Chem. 2023, 88, 14222-14226

Link: https://doi.org/10.1021/acs.joc.3c01534, opens an external URL in a new window

55.

“Cobalt Catalysts for [2+2+2] Cycloaddition Reactions: Isolated Precatalysts and in situ Generated Catalysts” (invited review)

T. Gläsel, B. Baumann, M. Hapke

Chem. Rec. 2021, 21, 3727-3745

Special Issue: Recent Advances in Transition‐Metal Catalysis, opens an external URL in a new window

Link: https://doi.org/10.1002/tcr.202100273, opens an external URL in a new window

54.

“CpCo(III) precatalysts for [2+2+2] cycloadditions”

F. Fischer, M. Eder, M. Hapke

Catalysts 2021, 11, 596

Link: https://doi.org/10.3390/catal11050596, opens an external URL in a new window

53. 

“Synthesis of Phosphinines from CoII-Catalyzed [2+1 2+2] Cycloaddition Reactions”

T. Gläsel, H. Jiao, M. Hapke

ACS Catal. 2021, 11, 13434-13444

Link: https://doi.org/10.1021/acscatal.1c03483, opens an external URL in a new window