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Prof. Dr. Marko Hapke

40. I. Thiel, H. Jiao, A. Spannenberg, M. Hapke, J. Organomet. Chem. 2014, 763-764, 60-64.
„Decomposition mechanism of a cobalt-coordinated phosphite-olefin ligand under irradiation”
DOI: 10.1016/j.jorganchem.2014.04.013
Link: http://www.sciencedirect.com/science/article/pii/S0022328X14001831

39. I. Thiel, M. Hapke, Rev. Inorg. Chem. 2014, 34, 217-245 (invited).
„The Broad Diversity of CpCo(I)-Complexes”
DOI: 10.1515/revic-2014-0001
Link:https://www.degruyter.com/abstract/j/revic.2014.34.issue-4/revic-2014-0001/revic-2014-0001.xml

38. I. Thiel, M. Hapke, J. Mol. Catal. A: Chem. 2014, 383-384, 153-158.
„The first solid-supported Cp’Co(I)-catalyst for the synthesis of pyridines”
DOI: 10.1016/j.molcata.2013.12.002
Link: http://www.sciencedirect.com/science/article/pii/S1381116913004585

37. C.-H. Guo, H.-S. Wu, M. Hapke, H. Jiao, J. Organomet. Chem. 2013, 748, 29-35.
„Theoretical studies on acetylene cyclotrimerization into benzene catalyzed by CpIr fragment“
DOI: 10.1016/j.jorganchem.2013.03.036
Link: http://www.sciencedirect.com/science/article/pii/S0022328X13002386

36. I. Thiel, A. Spannenberg, M. Hapke, ChemCatChem 2013, 5, 2865-2868.
„Synthesis of Air-Stable and Recyclable CpCoI-Complexes“
DOI: 10.1002/cctc.201300294
Link: http://dx.doi.org/10.1002/cctc.201300294

35. I. Thiel, M. Hapke, Angew. Chem. 2013, 125, 6030-6032; Angew. Chem. Int. Ed. 2013, 52, 5916-5918 (Highlight, invited).
„Computational Studies and Experimental Results—An Example of Excellent Teamwork in Studying Carbocyclization“
DOI: 10.1002/anie.201302496
Link: http://dx.doi.org/10.1002/anie.201302496

34. I. Thiel, M. Lamač, H. Jiao, A. Spannenberg, M. Hapke, Organometallics 2013, 32, 3415-3418.
„Synthesis and Catalytic Activity of [Cp’Co(COD)] Complexes Bearing Pendant N-Containing Groups”
DOI: 10.1021/om400330x
Link: http://dx.doi.org/10.1021/om400330x

33. M. Hapke, C. C. Tzschucke, Angew. Chem. 2013, 125, 3399-3401; Angew. Chem. Int. Ed. 2013, 52, 3317-3319.
„Achieving Enantioselectivity with Chiral Cyclopentadienylrhodium Complexes“ (Highlight)
DOI: 10.1002/anie.201209889
Link: http://dx.doi.org/10.1002/anie.201209889

32. I. Thiel, H. Jiao, A. Spannenberg, M. Hapke, Chem. Eur. J. 2013, 19, 2548-2554.
„Fine-Tuning the Reactivity and Stability by Systematic Ligand Variations in CpCo(I) Complexes as Catalysts for [2+2+2] Cycloaddition Reactions“
DOI: 10.1002/chem.201202946
Link: http://dx.doi.org/10.1002/chem.201202946

31. B. Heller, M. Hapke, C. Fischer, I. G. Stara, I. Stary, J. Organomet. Chem. 2013, 723, 98-102.
„Chiral cobaltI and nickel0 complexes in the synthesis of nonracemic helicenes through
enantioselective [2+2+2] cyclotrimerisation of alkynes”
DOI: 10.1016/j.jorganchem.2012.07.005
Link: http://www.sciencedirect.com/science/article/pii/S0022328X12004251

30. F. Fischer, P. Jungk, N. Weding, A. Spannenberg, H. Ott, M. Hapke, Eur. J. Org. Chem. 2012, 5828-5838.
„Diastereomeric Atropisomers from a Chiral Diyne by Co(I)-Catalyzed Cyclotrimerization”
DOI: 10.1002/ejoc.201200402
Link: http://dx.doi.org/10.1002/ejoc.201200402

29. N. Weding, A. Spannenberg, R. Jackstell, M. Hapke, Organometallics 2012, 31, 5660-5663.
“Formation and Reactivity of a Co4-µ-Alkyne Cluster from a Co(I)-Alkene Complex”
DOI: 10.1021/om300503y
Link: http://dx.doi.org/10.1021/om300503y

28. K. Kral, M. Hapke, Tetrahedron Lett. 2012, 53, 2856-2859.
„Investigations on the synthesis of monoarylated diynes by monoprotection/cross-
coupling/deprotection approach”
DOI: 10.1016/j.tetlet.2012.03.118
Link: http://www.sciencedirect.com/science/article/pii/S004040391200545X

27. N. Weding, R. Jackstell, H. Jiao, A. Spannenberg, M. Hapke, Adv. Synth. Catal. 2011, 353, 3423-3433.
„Synthesis of Group 9 Metal-Olefin Complexes with Identical Ligand Frameworks and
Comparison of their Catalytic Activity in [2+2+2] Cycloaddition and other Addition
Reactions”
DOI: 10.1002/adsc.201100489
Link: http://dx.doi.org/10.1002/adsc.201100489

26. N. Weding, M. Hapke, Chem. Soc. Rev. 2011, 40, 4525-4538 (invited).
„Preparation and synthetic applications of alkene complexes of group 9 transition metals in
[2+2+2] cycloaddition reactions”
DOI: 10.1039/C0CS00189A
Link: http://dx.doi.org/10.1039/C0CS00189A

25. K. Kral, M. Hapke, Angew. Chem. 2011, 123, 2482-2483; Angew. Chem. Int. Ed. 2011, 50, 2434-2435 (Highlight, invited).
„Metall-freie Cyclotrimerisierung zur De-novo-Synthese von Pyridinen“
DOI: 10.1002/anie.201007647
Link: http://dx.doi.org/10.1002/anie.201007647

24. M. Hapke, K. Kral, A. Spannenberg, Synthesis 2011, 642-652.
„On the Synthesis of Arylpropiolic Acid and Investigations towards the Formation of
Vinyl Chlorides by HCl Addition During Esterification Reactions”
DOI: 10.1055/s-0030-1258399
Link: https://www.thieme-connect.de/DOI/DOI?10.1055/s-0030-1258399

23. M. Hapke, N. Weding, A. Spannenberg, Organometallics 2010, 29, 4298-4304.
„Highly Reactive Cyclopentadienylcobalt (I) Olefin Complexes”
DOI: 10.1021/om100692k
Link: http://dx.doi.org/10.1021/om100692k

22. M. Hapke, N. Weding, A. Spannenberg, Acta Cryst. 2010, E66, m1031.
„Bis(dimethyl sulfoxide)hydridobis(triphenylphosphane)cobalt(I)”
DOI: 10.1107/S1600536810029466
Link: http://dx.doi.org/10.1107/S1600536810029466

21. M. Hapke, C. Fischer, K. Kral, A. Spannenberg, A. Gutnov, D. Redkin, B. Heller, J. Org. Chem. 2010, 75, 3993-4003.
„Asymmetric Synthesis of Axially Chiral 1-Aryl-5,6,7,8-tetrahydroquinolines by
Cobalt-Catalyzed [2+2+2] Cycloaddition Reaction of 1-Aryl-1,7-octadiynes and Nitriles”
DOI: 10.1021/jo100122d
Link: http://dx.doi.org/10.1021/jo100122d

20. K. R. Sawyer, J. F. Cahoon, J. E. Shanoski, E. A. Glascoe, M. F. Kling, J. P. Schlegel, M. C. Zoerb, M. Hapke, J. F. Hartwig, C. E. Webster, C. B. Harris, J. Am. Chem. Soc. 2010, 132, 1848-1859.
„Time-resolved IR Studies on the Mechanism for the Functionalization of Primary
C–H Bonds by Photoactivated Cp*W(CO)3(Bpin)”
DOI: 10.1021/ja906438a
Link: http://dx.doi.org/10.1021/ja906438a

19. M. Hapke, A. Gutnov, N. Weding, A. Spannenberg, C. Fischer, C. Benkhäuser-Schunk, B. Heller, Eur. J. Org. Chem. 2010, 509-514.
„Use of the Diels-Alder Cycloaddition of Tetracyclone and Internal Aryl Acetylenes for the
Synthesis of Functionalized Atropochiral Biaryls”
DOI: 10.1002/ejoc.200901080
Link: http://dx.doi.org/10.1002/ejoc.200901080

18. B. R. Aluri, N. Peulecke, B. H. Müller, S. Peitz, A. Spannenberg, M. Hapke, U. Rosenthal, Organometallics 2010, 29, 226-231.
„Synthesis, Coordination Chemistry, and Catalysis of the First 1,2-Bis(diphenylphosphino)-
1,2-diphenylhydrazine, Ph2PN(Ph)N(Ph)PPh2
DOI: 10.1021/om900925b
Link: http://dx.doi.org/10.1021/om900925b

17. J. Bunzen, M. Hapke, A. Lützen, Eur. J. Org. Chem. 2009, 3885-3894.
„The Influence of Different Spacer Lengths on the Selectivity of Self-Assembly Processes of
Bis(bipyridine)-BINOL Helicates”
DOI: 10.1002/ejoc.200900232
Link: http://dx.doi.org/10.1002/ejoc.200900232

16. M. Hapke, A. Wöhl, S. Peitz, A. Spannenberg, U. Rosenthal, Acta Cryst. 2009, E65, m357.
„trans-Di-µ-acetato-[µ-N,N-bis(diphenylphosphino)aniline]bis-[chloridomolybdenum(II)]
(Mo-Mo)-dichloro-methane-tetrahydrofuran (1/0.3/1.7)”
DOI: 10.1107/S1600536809007016
Link: http://dx.doi.org/10.1107/S1600536809007016

15. M. Hapke, A. Wöhl, S. Peitz, B. H. Müller, A. Spannenberg, U. Rosenthal, Acta Cryst. 2009, E65, m252.
„[N,N-bis(diphenylphosphino)isopropylamine]dibromidonickel(II)”
DOI: 10.1107/S1600536809003936
Link: http://dx.doi.org/10.1107/S1600536809003936

14. M. Hapke, A. Spannenberg, Acta Cryst. 2009, E65, m93.
„(η5-Cyclopentadienyl)bis(triphenylphosphane)-cobalt(I)-toluene-n-hexane (1/0.20/0.25))”
DOI: 10.1107/S1600536808042268
Link: http://dx.doi.org/10.1107/S1600536808042268

13. M. Hapke, L. Brandt, A. Lützen, Chem. Soc. Rev. 2008, 37, 2782-2797 (invited).
„Versatile tools in the construction of substituted 2,2'-bipyridines – cross-coupling reactions
with tin, zinc and boron compounds”
DOI: 10.1039/B810973G
Link: http://dx.doi.org/10.1039/B810973G

12. T. Schmidt, Z. Dai, H.-J. Drexler, M. Hapke, A. Preetz, D. Heller; Chem. Asian J. 2008, 3, 1170-1180.
„The Major/Minor Concept: Dependence of the Selectivity of Homogeneously Catalyzed
Reactions on Reactivity Ratio and Concentration Ratio of the Intermediates”
DOI: 10.1002/asia.200800023
Link: http://dx.doi.org/10.1002/asia.200800023

11. S. Enthaler, G. Erre, K. Junge, K. Schröder, D. Addis, D. Michalik, M. Hapke, D. Redkin, M. Beller, Eur. J. Org. Chem. 2008, 3352-3362.
„Iridium-Catalyzed Hydrogenation of β-Dehydroamino Acid Derivatives Using
Monodentate Phosphoramidites”
DOI: 10.1002/ejoc.200800241
Link: http://dx.doi.org/10.1002/ejoc.200800241

10. B. Heller, D. Redkin, A. Gutnov, C. Fischer, W. Bonrath, R. Karge, M. Hapke, Synthesis 2008, 69-74.
„Synthesis of Chiral Pyridyl Alcohols using a Two-Step Catalytic Approach”
DOI: 10.1055/s-2007-990903
Link: https://www.thieme-connect.de/DOI/DOI?10.1055/s-2007-990903

9. M. Hapke, H. Staats, I. Wallmann, A. Lützen, Synthesis 2007, 2711-2719.
„Synthesis of Amino-Functionalized 2,2’-Bipyridines”
DOI: 10.1055/s-2007-983824
Link:https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-2007-983824?lang=de

8. B. Heller, M. Hapke, Chem. Soc. Rev. 2007, 36, 1085-1094.
„The fascinating construction of pyridine ring systems by transition metal-catalysed
[2+2+2] cycloaddition reactions”
DOI: 10.1039/B607877J
Link: http://dx.doi.org/10.1039/B607877J

7. T. M. Boller, J. M. Murphy, M. Hapke, T. Ishiyama, N. Miyaura, J. F. Hartwig, J. Am. Chem. Soc. 2005, 127, 14263-14278.
„Mechanism of the Mild Functionalization of Arenes by Diboron Reagents Catalyzed
by Iridium Complexes. Intermediacy and Chemistry of Bipyridine-Ligated
Iridium Tris Boryl Complexes”
DOI: 10.1021/ja053433g
Link: http://dx.doi.org/10.1021/ja053433g

6. M. Albrecht, I. Janser, A. Lützen, M. Hapke, R. Fröhlich, P. Weis, Chem. Eur. J. 2005, 11, 5742-5748.
„5,5’-Diamino-2,2’-bipyridine: A versatile building block for the synthesis of
bipyridine/catechol ligands that form homo- and heteronuclear helicates"
DOI: 10.1002/chem.200401262
Link: http://dx.doi.org/10.1002/chem.200401262

5. J. F. Hartwig, K. S. Cook, M. Hapke, C. D. Incarvito, Y. Fan, C. E. Webster, M. B. Hall, J. Am. Chem. Soc. 2005, 127, 2538-2552.
„Rhodium Boryl Complexes in the Catalytic, Terminal Functionalization of Alkanes”
DOI: 10.1021/ja045090c
Link: http://dx.doi.org/10.1021/ja045090c

4. A. Lützen, M. Hapke, H. Staats, J. Bunzen, Eur. J. Org. Chem. 2003, 3948-3957.
„Synthesis of differently disubstituted 2,2’-bipyridines through a Modified Negishi
Cross-Coupling Reaction”
DOI: 10.1002/ejoc.200300192
Link: http://dx.doi.org/10.1002/ejoc.200300192

3. A. Lützen, M. Hapke, S. Meyer, Synthesis, 2002, 2289-2295.
„Synthesis of Bis(BINOL) Substituted 2,2’-Bipyridines and their Late
Transition Metal Complexes“
DOI: 10.1055/s-2002-34948
Link: https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-2002-34948

2. A. Lützen, M. Hapke, Eur. J. Org. Chem. 2002, 2292-2297.
„Synthesis of 5-substituted 2,2’-Bipyridines from Substituted 2-Chloropyridines by a
Modified Negishi Cross-Coupling Reaction“
DOI: 10.1002/1099-0690(200207)2002:14<2292::AID-EJOC2292>3.0.CO;2-D
Link:http://dx.doi.org/10.1002/1099-0690(200207)2002:14<2292::AID-EJOC2292>3.0.CO;2-D

1. A. Lützen, M. Hapke, J. Griep-Raming, D. Haase, W. Saak, Angew. Chem. 2002, 114, 2190-2194; Angew. Chem. Int. Ed. 2002, 41, 2086-2089.
„Synthese und stereoselektive Selbstorganisation von zwei- und dreisträngigen Helicaten“
DOI: 10.1002/1521-3773(20020617)41:12<2086::AID-ANIE2086>3.0.CO;2-0
Link:http://onlinelibrary.wiley.com/doi/10.1002/1521-3773%2820020617%2941:12%3C2086::AID-ANIE2086%3E3.0.CO;2-0/abstract