Publications

Peer reviewed articles

 

2019

1.         B. J. Elvers, C. Schulzke, and C. Fischer, Photochemical Unmasking of 1,3-Dithiol-2-ones: An Alternative Route to Heteroleptic Dithiolene Complexes from Low-Valent Molybdenum and Tungsten Precursors. Eur. J. Inorg. Chem., 2019, 0(23), p. 2796–2805. https://onlinelibrary.wiley.com/doi/abs/10.1002/ejic.201900124.

 

2.         N. Chrysochos, M. Ahmadi, S. Wahlefeld, Y. Rippers, I. Zebger, M. A. Mroginski, and C. Schulzke, Comparison of molybdenum and rhenium oxo bis-pyrazine-dithiolene complexes – in search of an alternative metal centre for molybdenum cofactor models. Dalton Trans., 2019, 48(8), p. 2701-2714. http://dx.doi.org/10.1039/C8DT04237C.

 

3.         R. Hofstetter, B. J. Elvers, F. Potlitz, A. Link, and C. Schulzke, Crystal structure of 7,8,15,16,17-pentathiadispiro[5.2.59.36]heptadecane. Acta Cryst. E, 2019, 75(6), p. 888-891. https://doi.org/10.1107/S2056989019007138.

 

4.         N. Muhammad, M. Ikram, S. Rehman, M. Ibrahim, S. Shujah, A. Wadood, S. Ali, M. Shah, Viola, Farzia, M. Ghufran, and C. Schulzke, Experimental and in silico DNA binding studies with easily accessible and stable zinc(II) carboxylates. J. Mol. Struct., 2019, 1187, p. 98-107. http://www.sciencedirect.com/science/article/pii/S0022286019303424.

 

5.         V. Zende, T. R. Girase, N. Chrysochos, C. Schulzke, and A. R. Kapdi, Amido-functionalized N-Heterocyclic carbene ligands and corresponding PalladiumComplexes: Synthesis, characterization and catalytic activity. J. Organomet. Chem., 2019, 888, p. 44-53. http://www.sciencedirect.com/science/article/pii/S0022328X19300932.

 

6.         B. Santra, D. Mandal, V. Gupta, P. Kalita, V. Kumar, R. S. Narayanan, A. Dey, N. Chrysochos, A. Mohammad, A. Singh, M. Zimmer, R. Dalapati, S. Biswas, C. Schulzke, V. Chandrasekhar, D. Scheschkewitz, and A. Jana, Structural Diversity in Supramolecular Organization of Anionic Phosphate Monoesters: Role of Cations. ACS Omega, 2019, 4(1), p. 2118-2133.

https://doi.org/10.1021/acsomega.8b03192.

 

2018

7.         V. Gupta, B. Santra, D. Mandal, S. Das, R. S. Narayanan, P. Kalita, D. K. Rao, C. Schulzke, S. K. Pati, V. Chandrasekhar, and A. Jana, Neutral and anionic phosphate-diesters as molecular templates for the encapsulation of a water dimer. Chem. Commun., 2018, 54(84), p. 11913-11916. http://dx.doi.org/10.1039/C8CC07138A.

 

8.         S. S. M. Bandaru, D. Dzubiel, H. Ihmels, M. Karbasiyoun, M. M. A. Mahmoud, and C. Schulzke, Synthesis of 9-arylalkynyl- and 9-aryl-substituted benzo[b]quinolizinium derivatives by Palladium-mediated cross-coupling reactions. Beilstein J. Org. Chem., 2018, 14, p. 1871-1884. https://www.beilstein-journals.org/bjoc/articles/14/161.

 

9.         S. Bhilare, S. S. Murthy Bandaru, J. Shah, N. Chrysochos, C. Schulzke, Y. S. Sanghvi, and A. R. Kapdi, Pd/PTABS: Low Temperature Etherification of Chloroheteroarenes. J. Org. Chem., 2018, 83, p. 13088 −13102. https://doi.org/10.1021/acs.joc.8b01840.

 

10.       V. Sable, K. Maindan, S. Bhilare, N. Chrysochos, C. Schulzke, and A. R. Kapdi, An Active Palladium Colloidal Catalyst for the Selective Oxidative Heterocoupling of (Hetero)Aryl Boronic Acids. Chem. Asian J., 2018, 13(17), p. 2489-2498. https://onlinelibrary.wiley.com/doi/abs/10.1002/asia.201800358.

 

11.       N. Chrysochos and C. Schulzke, Crystal structure of 1-ethyl-3-(2-oxo-1,3-dithiol-4-yl)quinoxalin-2(1H)-one. Acta Cryst. E, 2018, 74(7), p. 901-904. https://doi.org/10.1107/S2056989018007892.

 

12.       S. S. M. Bandaru, S. Bhilare, N. Chrysochos, V. Gayakhe, I. Trentin, C. Schulzke, and A. R. Kapdi, Pd/PTABS: Catalyst for Room Temperature Amination of Heteroarenes. Org. Lett., 2018, 20(2), p. 473-476. https://pubs.acs.org/doi/10.1021/acs.orglett.7b03854

 

13.       M. Ikram, M. Khan, S. Ahmad, S. Rehman, and C. Schulzke, The crystal structure of 4-tert-butyl-N′-[(E)-(4-fluoro-3-methoxyphenyl)methylidene]benzohydrazide, C19H21F1N2O2. Z. Kristallogr. - New Cryst. Struct., 2018, 233(4), p. 643-645. https://www.degruyter.com/view/j/ncrs.ahead-of-print/ncrs-2017-0408/ncrs-2017-0408.xml.

 

14.       S. S. M. Bandaru, A. R. Kapdi, and C. Schulzke, Crystal structure of 4-(pyrazin-2-yl)morpholine. Acta Cryst. E, 2018, 74(2), p. 137-140. https://doi.org/10.1107/S2056989018000312.

 

15.       S. Bhilare, S. S. M. Bandaru, A. R. Kapdi, Y. S. Sanghvi, and C. Schulzke, Pd/PTABS: An Efficient Water-Soluble Catalytic System for the Amination of 6-Chloropurine Ribonucleoside and Synthesis of Alogliptin. Curr. Protoc. Nucleic Acid Chem., 2018, 74(1), p. e58. https://currentprotocols.onlinelibrary.wiley.com/doi/abs/10.1002/cpnc.58.

 

16.       I. Trentin, C. Schindler, and C. Schulzke, Crystal structures of 4,4'-(disulfane-1,2-diyl)bis(5-methyl-2H-1,3-dithiol-2-one) and 4,4'-(diselanane-1,2-diyl)bis(5-methyl-2H-1,3-dithiol-2-one). Acta Cryst. E, 2018, 74(6), p. 840-845. https://doi.org/10.1107/S2056989018007454.

 

17.       M. Ikram, S. Rehman, A. Khan, and C. Schulzke, Crystal structure of the triethylammonium salt of 3-[(4-hydroxy-3-methoxyphenyl)(4-hydroxy-2-oxo-2H-chromen-3-yl)methyl]-2-oxo-2H-chromen-4-olate. Acta Cryst. E, 2018, 74(3), p. 282-286. https://doi.org/10.1107/S2056989018001561.

 

18.       A. V. Ardhapure, Y. S. Sanghvi, Y. Borozdina, A. R. Kapdi, and C. Schulzke, Crystal structure of 8-(4-methylphenyl)-2'-deoxyadenosine hemihydrate. Acta Cryst. E, 2018, 74(1), p. 1-5. https://doi.org/10.1107/S2056989017017212.

 

19.       V. Zende, T. R. Girase, N. Chrysochos, A. R. Kapdi, and C. Schulzke, Crystal structure of 1-butyl-3--1H-imidazol-3-ium chloride. Acta Cryst. E, 2018, 74(11), p. 1665-1668. https://doi.org/10.1107/S2056989018014792.

 

20.       N. Muhammad, M. Ikram, A. Wadood, S. Rehman, S. Shujah, Erum, M. Ghufran, S. Rahim, M. Shah, and C. Schulzke, Synthesis, crystal structure, DNA binding and molecular docking studies of zinc(II) carboxylates. Spectrochim. Acta, Part A, 2018, 190, p. 368-377.

http://www.sciencedirect.com/science/article/pii/S1386142517307369.

 

2017

21.       A. C. Ghosh, P. P. Samuel, and C. Schulzke, Synthesis, characterization and oxygen atom transfer reactivity of a pair of Mo(iv)O- and Mo(vi)O2-enedithiolate complexes - a look at both ends of the catalytic transformation. Dalton Trans., 2017, 46(23), p. 7523-7533. http://dx.doi.org/10.1039/C7DT01470H.

 

22.       D. Dhara, T. Vijayakanth, M. K. Barman, K. P. K. Naik, N. Chrysochos, C. B. Yildiz, R. Boomishankar, C. Schulzke, V. Chandrasekhar, and A. Jana, NHC-stabilized 1-hydrosilaimine: synthesis, structure and reactivity. Chem. Commun., 2017, 53(61), p. 8592-8595. http://dx.doi.org/10.1039/C7CC03912C.

 

23.       C. Schindler and C. Schulzke, The unexpected formation of a triselenide from 4-methyl-5-tri-n-butylstannyl-1,3-dithiol-2-one and selenium dioxide. Inorg. Chem. Commun., 2017, 77, p. 80-82. http://www.sciencedirect.com/science/article/pii/S1387700316305664.

 

24.       D. Mandal, B. Santra, P. Kalita, N. Chrysochos, A. Malakar, R. S. Narayanan, S. Biswas, C. Schulzke, V. Chandrasekhar, and A. Jana, 2,6-(Diphenylmethyl)-Aryl-Substituted Neutral and Anionic Phosphates: Approaches to H-Bonded Dimeric Molecular Structures. ChemistrySelect, 2017, 2(28), p. 8898-8910. http://dx.doi.org/10.1002/slct.201701133.

 

25.       A. V. A. Gholap, S. Maity, C. Schulzke, D. Maiti, and A. R. Kapdi, Synthesis of Cu-catalysed quinazolinones using a Csp3-H functionalisation/cyclisation strategy. Org. Biomol. Chem., 2017, 15(34), p. 7140-7146. http://dx.doi.org/10.1039/C7OB01723E.

 

26.       D. Mandal, R. Dolai, N. Chrysochos, P. Kalita, R. Kumar, D. Dhara, A. Maiti, R. S. Narayanan, G. Rajaraman, C. Schulzke, V. Chandrasekhar, and A. Jana, Stepwise Reversible Oxidation of N-Peralkyl-Substituted NHC-CAAC Derived Triazaalkenes: Isolation of Radical Cations and Dications. Org. Lett., 2017, 19(20), p. 5605-5608. https://pubs.acs.org/doi/10.1021/acs.orglett.7b02721.

 

27.       G. Dhangar, J. L. Serrano, C. Schulzke, K. C. Gunturu, and A. R. Kapdi, Palladacycle-Catalyzed Triple Suzuki Coupling Strategy for the Synthesis of Anthracene-Based OLED Emitters. ACS Omega, 2017, 2(7), p. 3144-3156. http://dx.doi.org/10.1021/acsomega.7b00725.

 

28.       P. Wawrzyniak, M. K. Kindermann, G. Thede, C. Schulzke, P. G. Jones, and J. W. Heinicke, Benzo/Naphtho-Anellated Dihydro-1,2-oxaphosphinines and Ring-Opening to P-Tertiary 2-Phosphanyl-1,1′-biaryl-2-ol Derivatives – Syntheses and Structures. Eur. J. Inorg. Chem., 2017, 2017(29), p. 3580-3586. http://dx.doi.org/10.1002/ejic.201700770.

 

29.       S. Perfahl, A. Bodtke, J. Pracharova, J. Kasparkova, V. Brabec, J. Cuadrado, S. Stürup, C. Schulzke, and P. J. Bednarski, Preparation of bis(5-phenyltetrazolato) Pt(II) and Pt(IV) analogues of transplatin and in vitro evaluation for antitumor activity. Inorg. Chim. Acta, 2017, 456, p. 86-94. http://www.sciencedirect.com/science/article/pii/S0020169316306247.

 

30.       S. Vojacek, K. Beese, Z. Alhalabi, S. Swyter, A. Bodtke, C. Schulzke, M. Jung, W. Sippl, and A. Link, Three-Component Aminoalkylations Yielding Dihydronaphthoxazine-Based Sirtuin Inhibitors: Scaffold Modification and Exploration of Space for Polar Side-Chains. Arch. Pharm., p. e201700097-n/a. http://dx.doi.org/10.1002/ardp.201700097.

 

31.       V. Gayakhe, A. R. Kapdi, Y. Borozdina, and C. Schulzke, Crystal structure of 5-(dibenzofuran-4-yl)-2'-deoxyuridine. Acta Cryst. E, 2017, 73(10), p. 1493-1496. https://doi.org/10.1107/S2056989017013111.

 

32.       U. Schulz, A. Grossmann, F. Wilde, M. Freitag, C. Lemmerhirt, C. Schulzke, A. Link, and O. Morgenstern, Synthesis, chemical behavior, structure elucidation and iNOS inhibitory activity of 1-substituted 3-methylsulfanyl-5,6,7,8-tetrahydro-1H-[1,2,4]triazolo[1,2-a]pyridazines+. Pharmazie, 2017, 72(7), p. 371-382. https://doi.org/10.1691/ph.2017.6902.

 

33.       K. R. Basvani, M. K. Kindermann, H. Frauendorf, C. Schulzke, P. G. Jones, and J. W. Heinicke, 3-Phenylphosphaprolines – Synthesis, structure and properties of heterocyclic α-phosphanyl amino acids. Polyhedron, 2017, 130, p. 195-204.

http://www.sciencedirect.com/science/article/pii/S0277538717302838.

 

2016

34.       A. C. Ghosh and C. Schulzke, Selectively detecting Hg2+ – A “mercury quick test” with bis-(coumarin–dithiolene) niccolate. Inorg. Chim. Acta, 2016, 445, p. 149-154. http://www.sciencedirect.com/science/article/pii/S0020169316300792.

 

35.       A. C. Ghosh, K. Weisz, and C. Schulzke, Selective Capture of Ni2+ Ions by Naphthalene- and Coumarin-Substituted Dithiolenes. Eur. J. Inorg. Chem., 2016, 2016(2), p. 208-218. http://dx.doi.org/10.1002/ejic.201500847.

 

36.       S. Bhilare, V. Gayakhe, A. V. Ardhapure, Y. S. Sanghvi, C. Schulzke, Y. Borozdina, and A. R. Kapdi, Novel water-soluble phosphatriazenes: versatile ligands for Suzuki-Miyaura, Sonogashira and Heck reactions of nucleosides. RSC Advances, 2016, 6(87), p. 83820-83830. http://dx.doi.org/10.1039/C6RA19039A.

 

37.       D. Dhara, D. Mandal, A. Maiti, C. B. Yildiz, P. Kalita, N. Chrysochos, C. Schulzke, V. Chandrasekhar, and A. Jana, Assembly of NHC-stabilized 2-hydrophosphasilenes from Si(iv) precursors: a Lewis acid-base complex. Dalton Trans., 2016, 45(48), p. 19290-19298. http://dx.doi.org/10.1039/C6DT04321F.

 

38.       V. Gayakhe, A. Ardhapure, A. R. Kapdi, Y. S. Sanghvi, J. L. Serrano, L. García, J. Pérez, J. García, G. Sánchez, C. Fischer, and C. Schulzke, Water-Soluble Pd–Imidate Complexes: Broadly Applicable Catalysts for the Synthesis of Chemically Modified Nucleosides via Pd-Catalyzed Cross-Coupling. J. Org. Chem., 2016, 81(7), p. 2713-2729. http://dx.doi.org/10.1021/acs.joc.5b02475.

 

39.       T. Guchhait, G. Mani, and C. Schulzke, Synthesis and structural characterization of anion complexes with azacalix[2]dipyrrolylmethane: effect of anion charge on the conformation of the macrocycle. Dalton Trans., 2016, 45(29), p. 11781-11790. http://dx.doi.org/10.1039/C6DT01396A.

 

40.       N. Muhammad, M. Ikram, S. Rehman, M. Ibrahim Viola, and C. Schulzke, Structural, thermal kinetics and thermodynamics study of new mixed ligand zinc complexes. J. Therm. Anal. Calorim., 2016, p. 1-11. http://dx.doi.org/10.1007/s10973-016-5842-7.

 

41.       S. Perfahl, M. M. Natile, H. S. Mohamad, C. A. Helm, C. Schulzke, G. Natile, and P. J. Bednarski, Photoactivation of Diiodido–Pt(IV) Complexes Coupled to Upconverting Nanoparticles. Molecular Pharmaceutics, 2016, 13(7), p. 2346-2362. http://dx.doi.org/10.1021/acs.molpharmaceut.6b00108.

 

42.       V. Gayakhe, A. V. Ardhapure, A. R. Kapdi, Y. S. Sanghvi, J. L. Serrano, and C. Schulzke, C-C Bond Formation: Synthesis of C5 Substituted Pyrimidine and C8 Substituted Purine Nucleosides Using Water Soluble Pd-imidate Complex. Curr. Protoc. Nucleic Acid Chem., 2016(65), p. 1.37.1-1.37.15.

http://dx.doi.org/10.1002/cpnc.1.

 

2015

43.       S. P. Sarish, P. P. Samuel, H. W. Roesky, C. Schulzke, K. Nijesh, S. De, and P. Parameswaran, Multiple Cycloaddition Reactions of Ketones with a β-Diketiminate Al Compound. Chem. Eur. J., 2015, 21(52), p. 19041-19047. http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201503137/abstract.

 

44.       C. Schindler and C. Schulzke, Pyrazine- and pyridine-substituted prop-2-yn-1-ols, but-3-yn-2-ols, and but-3-yn-2-ones – purification, stability, and handling revised. Chem. Heterocycl. Compd., 2015, 51((11/12)), p. 1008-1013. http://dx.doi.org/10.1007/s10593-016-1811-0.

 

45.       J. P. Dicks, M. Zubair, E. S. Davies, C. D. Garner, C. Schulzke, C. Wilson, and J. McMaster, Synthesis, Structure and Redox Properties of Asymmetric (Cyclopentadienyl)(ene-1,2-dithiolate)cobalt(III) Complexes Containing Phenyl, Pyridyl and Pyrazinyl Units. Eur. J. Inorg. Chem., 2015, 2015(21), p. 3550-3561. http://dx.doi.org/10.1002/ejic.201500138.

 

46.       M. Ghalib, P. G. Jones, C. Schulzke, D. Sziebert, L. Nyulászi, and J. W. Heinicke, π-Rich σ2P-Heterocycles: Bent η1-P- and μ2-P-Coordinated 1,3-Benzazaphosphole Copper(I) Halide Complexes. Inorg. Chem., 2015, 54(5), p. 2117-2127. http://dx.doi.org/10.1021/ic502367d.

 

47.       M. Ghalib, L. Konczol, L. Nyulaszi, G. J. Palm, C. Schulzke, and J. W. Heinicke, [small pi]-Excess aromatic [sigma]2-P ligands: synthesis and structure of an unprecedented [small mu ]2-P-1,3-benzazaphosphole bridged tetranuclear copper(i) acetate complex. Dalton Trans., 2015, 44(4), p. 1769-1774. http://dx.doi.org/10.1039/C4DT03072A.

 

48.       M. Ghalib, C. Schulzke, G. J. Palm, and J. W. Heinicke, π-Excess aromatic σ2P ligands: Unprecedented reductive C–C coupling of neopentylbenzazaphosphole at the PCH–N group by Fe3(CO)12 to an heterocyclic 1,2-bis(phosphido)-Fe2(CO)6 complex. J. Organomet. Chem., 2015, 776(0), p. 60-63. http://www.sciencedirect.com/science/article/pii/S0022328X14005361.

 

49.       M. Ikram, S. Rehman, A. Khan, R. J. Baker, T. S. Hofer, F. Subhan, M. Qayum, Faridoon, and C. Schulzke, Synthesis, characterization, antioxidant and selective xanthine oxidase inhibitory studies of transition metal complexes of novel amino acid bearing Schiff base ligand. Inorg. Chim. Acta, 2015, 428(0), p. 117-126. http://www.sciencedirect.com/science/article/pii/S0020169315000249.

 

50.       A. Nobili, F. Steffen-Munsberg, H. Kohls, I. Trentin, C. Schulzke, M. Höhne, and U. T. Bornscheuer, Engineering the Active Site of the Amine Transaminase from Vibrio fluvialis for the Asymmetric Synthesis of Aryl–Alkyl Amines and Amino Alcohols. ChemCatChem, 2015, 7(5), p. 757–760. http://dx.doi.org/10.1002/cctc.201403010.

 

51.       D. Prajapati, C. Schulzke, M. K. Kindermann, and A. R. Kapdi, Selective palladium-catalysed arylation of 2,6-dibromopyridine using N-heterocyclic carbene ligands. RSC Advances, 2015, 5(65), p. 53073-53085. http://dx.doi.org/10.1039/C5RA10561G.

 

52.       P. Schrapers, T. Hartmann, R. Kositzki, H. Dau, S. Reschke, C. Schulzke, S. Leimkühler, and M. Haumann, Sulfido and Cysteine Ligation Changes at the Molybdenum Cofactor during Substrate Conversion by Formate Dehydrogenase (FDH) from Rhodobacter capsulatus. Inorg. Chem., 2015, 54(7), p. 3260-3271. http://dx.doi.org/10.1021/ic502880y.

 

53.       V. M. Zende, C. Schulzke, and A. R. Kapdi, Pincer CNC bis-N-heterocyclic carbenes: robust ligands for palladium-catalysed Suzuki-Miyaura arylation of bromoanthracene and related substrates. Organic Chemistry Frontiers, 2015, 2(10), p. 1397-1410.

http://dx.doi.org/10.1039/C5QO00236B.

 

2014 and earlier

54.       A. C. Ghosh, J. K. Reinhardt, M. K. Kindermann, and C. Schulzke, The ring opening reaction of 1,3-dithiol-2-one systems is fully reversible. Chem. Commun., 2014, 50(70), p. 10102-10104. http://dx.doi.org/10.1039/C4CC04414B.

 

55.       E. Hashem, T. McCabe, C. Schulzke, and R. J. Baker, Synthesis, structure and photophysical properties of [UO2X2(O=PPh3)2] (X = Cl, Br, I). Dalton Trans., 2014, 43(3), p. 1125-1131. http://dx.doi.org/10.1039/C3DT52480A.

 

56.       E. Hashem, J. A. Platts, F. Hartl, G. Lorusso, M. Evangelisti, C. Schulzke, and R. J. Baker, Thiocyanate Complexes of Uranium in Multiple Oxidation States: A Combined Structural, Magnetic, Spectroscopic, Spectroelectrochemical, and Theoretical Study. Inorg. Chem., 2014, 53(16), p. 8624-8637. http://dx.doi.org/10.1021/ic501236j.

 

57.       A. Döring, C. Fischer, and C. Schulzke, Mono-oxo-bis-dithioveratrol-molybdate – in Solution a Model for Arsenite Oxidase and in the Solid State a Coordination Polymer with Unprecedented Binding Motifs. Z. Anorg. Allg. Chem., 2013, p. 1552-1558. http://dx.doi.org/10.1002/zaac.201300076.

 

58.       M. Zubair, A. C. Ghosh, and C. Schulzke, The unexpected and facile molybdenum mediated formation of tri- and tetracyclic pentathiepins from pyrazine-alkynes and sulfur. Chem. Commun., 2013, 49(39), p. 4343-4345. http://pubs.rsc.org/en/content/articlepdf/2013/cc/c2cc37025e.

 

59.       E. Hashem, G. Lorusso, M. Evangelisti, T. McCabe, C. Schulzke, J. A. Platts, and R. J. Baker, Fingerprinting the oxidation state of U(iv) by emission spectroscopy. Dalton Trans., 2013, 42(41), p. 14677-14680. http://dx.doi.org/10.1039/C3DT52151F.

 

60.       E. Hashem, A. N. Swinburne, C. Schulzke, R. C. Evans, J. A. Platts, A. Kerridge, L. S. Natrajan, and R. J. Baker, Emission spectroscopy of uranium(iv) compounds: a combined synthetic, spectroscopic and computational study. RSC Advances, 2013, 3(13), p. 4350-4361. http://dx.doi.org/10.1039/C3RA22712J.

 

61.       M. Ikram, S. Rehman, M. Ali, Faridoon, C. Schulzke, R. J. Baker, A. J. Blake, K. Malook, H. Wong, and R. Saeed Ur, Urease and α-chymotrypsin inhibitory activities of transition metal complexes of new Schiff base ligand: Kinetic and thermodynamic studies of the synthesized complexes using TG–DTA pyrolysis. Thermochim. Acta, 2013, 562(0), p. 22-28. http://www.sciencedirect.com/science/article/pii/S0040603113001603.

 

62.       D. Jana, G. Mani, and C. Schulzke, Synthesis of Novel Polyazacryptands for Recognition of Tetrahedral Oxoanions and Their X-ray Structures. Inorg. Chem., 2013, 52(11), p. 6427-6439. http://dx.doi.org/10.1021/ic400319b.

 

63.       A. R. Kapdi, A. Karbelkar, M. Naik, S. Pednekar, C. Fischer, C. Schulzke, and M. Tromp, Efficient synthesis of coumarin-based tetra and pentacyclic rings using phospha-palladacycles. RSC Advances, 2013, 3(43), p. 20905-20912. http://dx.doi.org/10.1039/C3RA43821J.

 

64.       X. Ma and C. Schulzke, Molybdenum and tungsten complexes of bis(phenolate) ligands, O,X,O (X = S or Se): Synthesis, characterization and catalytic oxygen atom transfer properties. Inorg. Chim. Acta, 2013, 395(0), p. 218-224. http://www.sciencedirect.com/science/article/pii/S0020169312006457.

 

65.       S. Reschke, K. G. V. Sigfridsson, P. Kaufmann, N. Leidel, S. Horn, K. Gast, C. Schulzke, M. Haumann, and S. Leimkühler, Identification of a Bis-molybdopterin Intermediate in Molybdenum Cofactor Biosynthesis in Escherichia coli. J. Biol. Chem., 2013, 288(41), p. 29736-29745. http://www.jbc.org/content/288/41/29736.abstract.

 

66.       T. Guchhait, G. Mani, C. Schulzke, and A. Anoop, A Tripyrrolylmethane-Based Macrobicyclic Triazacryptand: X-ray Structure, Size-Selective Anion Binding, and Fluoride-Ion-Mediated Proton–Deuterium Exchange Studies. Inorg. Chem., 2012, 51(21), p. 11635-11644. http://pubs.acs.org/doi/abs/10.1021/ic301546v.

 

67.       M. Ikram, R. Saeed Ur, S. Rehman, R. J. Baker, and C. Schulzke, Synthesis, characterization and distinct butyrylcholinesterase activities of transition metal complexes of 2-[(E)-(quinolin-3-ylimino)methyl]phenol. Inorg. Chim. Acta, 2012, 390(0), p. 210-216. http://www.sciencedirect.com/science/article/pii/S0020169312002952.

 

68.       A. Mukherjee, T. K. Sen, P. K. Ghorai, P. P. Samuel, C. Schulzke, and S. K. Mandal, Phenalenyl-Based Organozinc Catalysts for Intramolecular Hydroamination Reactions: A Combined Catalytic, Kinetic, and Mechanistic Investigation of the Catalytic Cycle. Chem. Eur. J., 2012, 18(34), p. 10530-10545. http://dx.doi.org/10.1002/chem.201200868.

 

69.       C. Schulzke, Molybdenum and Tungsten Oxidoreductase Models. Eur. J. Inorg. Chem., 2011, 2011(8), p. 1189-1199. http://dx.doi.org/10.1002/ejic.201001036.

 

70.       L. Ackermann, A. R. Kapdi, S. Fenner, C. Kornhaaß, and C. Schulzke, Well-Defined Air-Stable Palladium HASPO Complexes for Efficient Kumada–Corriu Cross-Couplings of (Hetero)Aryl or Alkenyl Tosylates. Chem. Eur. J., 2011, 17(10), p. 2965-2971. http://dx.doi.org/10.1002/chem.201002386.

 

71.       J. Baker, R. Baker, and C. Schulzke, Perfluorinated oxygen- and sulfur-containing compounds as extractants for gold(III). Gold Bulletin, 2011, 44(2), p. 79-83. http://link.springer.com/content/pdf/10.1007%2Fs13404-011-0011-z.pdf.

 

72.       K. G. V. Havelius, S. Reschke, S. Horn, A. Döring, D. Niks, R. Hille, C. Schulzke, S. Leimkühler, and M. Haumann, Structure of the Molybdenum Site in YedY, a Sulfite Oxidase Homologue from Escherichia coli. Inorg. Chem., 2011, 50(3), p. 741-748. http://dx.doi.org/10.1021/ic101291j.

 

73.       A. Jana, R. Azhakar, S. P. Sarish, P. P. Samuel, H. W. Roesky, C. Schulzke, and D. Koley, Reactions of Stable Amidinate Chlorosilylene and [1+4]-Oxidative Addition of N-Heterocyclic Silylene with N-Benzylideneaniline. Eur. J. Inorg. Chem., 2011, 2011(32), p. 5006-5013. http://onlinelibrary.wiley.com/doi/10.1002/ejic.201100661/abstract.

 

74.       F. Kanaan, C. Schulzke, K. Strüber, and U. Klingebiel, 2-Lithiumamide-2-fluoro-1,3-diaza-2,4-disilacyclobutanes – Syntheses, Reactions, Structures. Z. Anorg. Allg. Chem., 2011, 637(14-15), p. 2183-2192. http://onlinelibrary.wiley.com/doi/10.1002/zaac.201100346/abstract.

 

75.       A. Mukherjee, T. Sen, S. Mandal, D. Kratzert, D. Stalke, A. Döring, and C. Schulzke, Phenalenyl-based ligand for transition metal chemistry: Application in Henry reaction. J. Chem. Sci., 2011, 123(2), p. 139-144. http://link.springer.com/article/10.1007%2Fs12039-011-0107-2.

 

76.       P. P. Samuel, S. Horn, A. Döring, K. G. V. Havelius, S. Reschke, S. Leimkühler, M. Haumann, and C. Schulzke, A Crystallographic and Mo K-Edge XAS Study of Molybdenum Oxo Bis-, Mono-, and Non-Dithiolene Complexes – First-Sphere Coordination Geometry and Noninnocence of Ligands. Eur. J. Inorg. Chem., 2011, 2011(28), p. 4387-4399. http://dx.doi.org/10.1002/ejic.201100331.

 

77.       S. P. Sarish, A. Jana, H. W. Roesky, P. P. Samuel, C. E. A. Andrade, B. Dittrich, and C. Schulzke, Synthesis of a Lewis Base Stabilized Dimer of N-Substituted Hydrosila Hydrazone and a Silaaziridine. Organometallics, 2011, 30(4), p. 912-916. http://pubs.acs.org/doi/abs/10.1021/om101066w.

 

78.       C. E. Abad Andrade, X. Ma, W. Meyer-Klaucke, and C. Schulzke, The difference one ligand atom makes - An altered oxygen transfer reaction mechanism caused by an exchange of selenium for sulfur. Polyhedron, 2010, 29(1), p. 664-668. http://www.sciencedirect.com/science/article/pii/S0277538709006834.

 

79.       A. Döring and C. Schulzke, Tungsten's redox potential is more temperature sensitive than that of molybdenum. Dalton Trans., 2010, 39(24), p. 5623-5629. http://pubs.rsc.org/en/Content/ArticleLanding/2010/DT/c000489h.

 

80.       A. Döring, C. Schulzke, and Q. Zhang, Synthesis, characterization and structural analysis of isostructural dinuclear molybdenum and tungsten oxo-bis-mu-sulfido-benzenedithiolene complexes. Inorg. Chim. Acta, 2010, 363(14), p. 4140-4144. http://www.sciencedirect.com/science/article/pii/S0020169310003440.

 

81.       L. Ackermann, A. R. Kapdi, and C. Schulzke, Air-Stable Secondary Phosphine Oxide or Chloride (Pre)Ligands for Cross-Couplings of Unactivated Alkyl Chlorides. Org. Lett., 2010, 12(10), p. 2298-2301. http://dx.doi.org/10.1021/ol100658y.

 

82.       L. Ackermann, H. K. Potukuchi, A. R. Kapdi, and C. Schulzke, Kumada–Corriu Cross-Couplings with 2-Pyridyl Grignard Reagents. Chem. Eur. J., 2010, 16(11), p. 3300-3303. http://dx.doi.org/10.1002/chem.201000032.

 

83.       R. S. Ghadwal, H. W. Roesky, C. Schulzke, and M. Granitzka, N-Heterocyclic Carbene Stabilized Dichlorosilaimine IPr·Cl2Si═NR. Organometallics, 2010, 29(23), p. 6329-6333. http://pubs.acs.org/doi/abs/10.1021/om100737v.

 

84.       M. Görth, U. Schneider, H. Ott, C. Schulzke, D. Stalke, and U. Klingebiel, Synthesis and Cyclisation of Boryl- and Silylhydrazones. Zeitschrift Fur Naturforschung Section B-a Journal of Chemical Sciences, 2010, 65(5), p. 587-602. http://www.znaturforsch.com/ab/v65b/65b0587.pdf.

 

85.       A. Jana, H. W. Roesky, and C. Schulzke, Reactivity of germanium(II) hydride with nitrous oxide, trimethylsilyl azide, ketones, and alkynes and the reaction of a methyl analogue with trimethylsilyl diazomethane. Dalton Trans., 2010, 39(1), p. 132-138. http://pubs.rsc.org/en/Content/ArticleLanding/2010/DT/b914164b.

 

86.       A. Jana, H. W. Roesky, C. Schulzke, and P. P. Samuel, An Efficient Route for the Synthesis of a Tin(II) Substituted Carbodiimide from a Diazo Compound. Inorg. Chem., 2010, 49(7), p. 3461-3464. http://pubs.acs.org/doi/abs/10.1021/ic100031d.

 

87.       A. Jana, H. W. Roesky, C. Schulzke, and P. P. Samuel, Reaction of Tin(II) Hydride with Compounds Containing Aromatic C−F Bonds. Organometallics, 2010, 29(21), p. 4837-4841. http://pubs.acs.org/doi/abs/10.1021/om1000106.

 

88.       A. Jana, H. W. Roesky, C. Schulzke, P. P. Samuel, and A. Döring, Synthesis and Reaction of Monomeric Germanium(II) and Lead(II) Dimethylamide and the Synthesis of Germanium(II) Hydrazide by Clevage of one N−H bond of Hydrazine. Inorg. Chem., 2010, 49(12), p. 5554-5559. http://pubs.acs.org/doi/abs/10.1021/ic1003808.

 

89.       A. Jana, P. P. Samuel, H. W. Roesky, and C. Schulzke, Preparation of iron carbonyl complexes of germanium(II) and tin(II) each with a terminal fluorine atom. J. Fluorine Chem., 2010, 131(11), p. 1096-1099. http://www.sciencedirect.com/science/article/pii/S0022113910000801.

 

90.       A. Jana, P. P. Samuel, G. Tavčar, H. W. Roesky, and C. Schulzke, Selective Aromatic C−F and C−H Bond Activation with Silylenes of Different Coordinate Silicon. J. Am. Chem. Soc., 2010, 132(29), p. 10164-10170. http://pubs.acs.org/doi/abs/10.1021/ja103988d.

 

91.       A. Jana, S. P. Sarish, H. W. Roesky, C. Schulzke, and P. P. Samuel, A rational design for an efficient synthesis of a monomeric tin(ii). Chem. Commun., 2010, 46(5), p. 707-709. http://pubs.rsc.org/en/Content/ArticleLanding/2010/CC/b920306k.

 

92.       A. Jana, G. Tavčar, H. W. Roesky, and C. Schulzke, Facile synthesis of dichlorosilane by metathesis reaction and dehydrogenation of dihydrogermane by a frustrated Lewis pair. Dalton Trans., 2010, 39(27), p. 6217-6220. http://pubs.rsc.org/en/Content/ArticleLanding/2010/DT/c002395g.

 

93.       J. Li, C. Schulzke, S. Merkel, Herbert W. Roesky, Prinson P. Samuel, A. Döring, and D. Stalke, Synthesis and Characterization of N-heterocyclic Carbene Complexes of Titanium(IV) and Titanium(III) Z. Anorg. Allg. Chem., 2010, 636(3-4), p. 511-514. http://onlinelibrary.wiley.com/doi/10.1002/zaac.200900486/pdf.

 

94.       N. D. Reddy, A. Jana, H. W. Roesky, P. P. Samuel, and C. Schulzke, Synthesis of phosphine substituted [small beta]-diketiminate based isomeric Ge(ii). Dalton Trans., 2010, 39(1), p. 234-238. http://pubs.rsc.org/en/Content/ArticleLanding/2010/DT/b915403e.

 

95.       X. Ma, Z. Yang, and C. Schulzke, Crystal structure of bis(1,3-diisopropyl-4,5-dimethylimidazolium) hexamolybdate, [C11H21N2]2[Mo6O19] Zeitschrift für Kristallographie – New Crystal Structures 2010, 225(4), p. 775-776. ftp://ftp.oldenbourg.de/pub/download/frei/ncs/225-4/1267-3217.pdf.

 

96.       U. Ryde, C. Schulzke, and K. Starke, Which functional groups of the molybdopterin ligand should be considered when modeling the active sites of the molybdenum and tungsten cofactors? A density functional theory study. J. Biol. Inorg. Chem., 2009, 14(7), p. 1053-1064. http://dx.doi.org/10.1007/s00775-009-0548-y.

 

97.       C. Schulzke, Temperature dependent electrochemistry-a versatile tool for investigations of biology related topics. Dalton Trans., 2009(34), p. 6683-6691. http://pubs.rsc.org/en/Content/ArticleLanding/2009/DT/b904361f.

 

98.       A. Jana, B. Nekoueishahraki, H. W. Roesky, and C. Schulzke, Stable Compounds of Composition LGe(II)R (R = OH, PhO, C6F5O, PhCO2) Prepared by Nucleophilic Addition Reactions. Organometallics, 2009, 28(13), p. 3763-3766. http://pubs.acs.org/doi/abs/10.1021/om900149k.

 

99.       A. Jana, H. W. Roesky, and C. Schulzke, Hydrostannylation of Ketones and Alkynes with LSnH [L = HC(CMeNAr)2, Ar = 2,6-iPr2C6H3]. Inorg. Chem., 2009, 48(19), p. 9543-9548. http://pubs.acs.org/doi/abs/10.1021/ic9012069.

 

100.     A. Jana, H. W. Roesky, C. Schulzke, and A. Döring, Reactions of Tin(II) Hydride Species with Unsaturated Molecules. Angew. Chem., 2009, 121(6), p. 1126-1129. http://onlinelibrary.wiley.com/doi/10.1002/ange.200805595/abstract.

 

101.     A. Jana, H. W. Roesky, C. Schulzke, A. Döring, T. Beck, A. Pal, and R. Herbst-Irmer, Facile Access of Stable Divalent Tin Compounds with Terminal Methyl, Amide, Fluoride, and Iodide Substituents. Inorg. Chem., 2009, 48(1), p. 193-197. http://pubs.acs.org/doi/abs/10.1021/ic8015639.

 

102.     A. Jana, H. W. Roesky, C. Schulzke, and P. P. Samuel, Insertion Reaction of a Silylene into a N−H Bond of Hydrazine and a [1+4] Cycloaddition with Diphenyl Hydrazone. Organometallics, 2009, 28(22), p. 6574-6577. http://pubs.acs.org/doi/abs/10.1021/om9007086.

 

103.     A. Jana, S. P. Sarish, H. W. Roesky, C. Schulzke, A. Döring, and M. John, Facile Access of Well-Defined Stable Divalent Lead Compounds with Small Organic Substituents. Organometallics, 2009, 28(8), p. 2563-2567. http://pubs.acs.org/doi/abs/10.1021/om801167c.

 

104.     A. Jana, C. Schulzke, and H. W. Roesky, Oxidative Addition of Ammonia at a Silicon(II) Center and an Unprecedented Hydrogenation Reaction of Compounds with Low-Valent Group 14 Elements Using Ammonia Borane. J. Am. Chem. Soc., 2009, 131(13), p. 4600-4601. http://pubs.acs.org/doi/abs/10.1021/ja900880z.

 

105.     A. Jana, S. S. Sen, H. W. Roesky, C. Schulzke, S. Dutta, and S. K. Pati, End-On Nitrogen Insertion of a Diazo Compound into a Germanium(II) Hydrogen Bond and a Comparable Reaction with Diethyl Azodicarboxylate. Angew. Chem., Int. Ed., 2009, 48(23), p. 4246-4248. http://onlinelibrary.wiley.com/doi/10.1002/anie.200900617/abstract.

 

106.     X. Ma, Z. Yang, C. Schulzke, M. Noltemeyer, and H.-G. Schmidt, Synthesis, structure and characterization of a new tetrameric tungsten-oxo complex WO2Cl2(THF) (4). Inorg. Chim. Acta, 2009, 362(15), p. 5275-5277. http://www.sciencedirect.com/science/article/pii/S0020169309005295.

 

107.     B. Nekoueishahraki, S. P. Sarish, H. W. Roesky, D. Stern, C. Schulzke, and D. Stalke, Addition of Dimethylaminobismuth to Aldehydes, Ketones, Alkenes, and Alkynes. Angew. Chem., 2009, 121(25), p. 4587-4590. http://onlinelibrary.wiley.com/doi/10.1002/ange.200901215/abstract.

 

108.     S. S. Sen, A. Jana, H. W. Roesky, and C. Schulzke, A Remarkable Base-Stabilized Bis(silylene) with a Silicon(I)-Silicon(I) Bond. Angew. Chem., Int. Ed., 2009, 48(45), p. 8536-8538. http://onlinelibrary.wiley.com/doi/10.1002/anie.200902995/abstract.

 

109.     X. Ma, C. Schulzke, H.-G. Schmidt, and M. Noltemeyer, Structural, electrochemical and oxygen atom transfer properties of a molybdenum selenoether complex [Mo2O4(OC3H6SeC3H6O)2] and its thioether analogue [Mo2O4(OC3H6SC3H6O)2]. Dalton Trans., 2007(18), p. 1773-1780. http://pubs.rsc.org/en/Content/ArticleLanding/2007/DT/b617652f.

 

110.     X. Ma, C. Schulzke, Z. Yang, A. Ringe, and J. Magull, Synthesis, structures and oxygen atom transfer catalysis of oxo-bridged molybdenum(V) complexes with heterocyclic bidentate ligands (N,X) X = S, Se. Polyhedron, 2007, 26(18), p. 5497-5505. http://www.sciencedirect.com/science/article/pii/S0277538707004974.

 

111.     X. Ma, Z. Yang, C. Schulzke, A. Ringe, and J. Magull, The Monomerization of a Binuclear Molybdenum(VI) Dioxo Complex by an Unusual Silylation Reaction. Z. Anorg. Allg. Chem., 2007, 633(9), p. 1320-1322. http://onlinelibrary.wiley.com/doi/10.1002/zaac.200700125/abstract.

 

112.     Q. Zhang, C. Schulzke, H.-G. Schmidt, and M. Noltemeyer, Crystal structure of dimethylformamide-diethanolateamine-dioxomolybdenum(VI),MoO2 O(CH2)(2)NH (CH2)(2)O (CH3)(2)NCHO. Zeitschrift Fur Kristallographie-New Crystal Structures, 2007, 222(3), p. 215-216. http://www.oldenbourg.de/verlag/zkristallogr/mn-ncsc0703.htm.

 

113.     Q. Zhang, K. Starke, C. Schulzke, A. Hofmeister, and J. Magull, Different reaction behaviour of molybdenum and tungsten - Reactions of the dichloro dioxo dimethyl-bispyridine complexes with thiophenolate. Inorg. Chim. Acta, 2007, 360(10), p. 3400-3407. http://www.sciencedirect.com/science/article/pii/S0020169307002721.

 

114.     X. Ma, K. Starke, C. Schulzke, H.-G. Schmidt, and M. Noltemeyer, Structural, Electrochemical, and Theoretical Investigations of New Thio- and Selenoether Complexes of Molybdenum and Tungsten. Eur. J. Inorg. Chem., 2006, 2006(3), p. 628-637. http://onlinelibrary.wiley.com/doi/10.1002/ejic.200500698/abstract.

 

115.     X. Ma, Z. Yang, C. Schulzke, H.-G. Schmidt, and M. Noltemeyer, An unprecedented example of polyoxotungstates: Synthesis and characterization of an octatungstate complex W8O19L3(acac)(4) (L = O-(CH2)(3)S(CH2)(3)O-). Inorg. Chem. Commun., 2006, 9(8), p. 777-781. http://www.sciencedirect.com/science/article/pii/S1387700306001614.

 

116.     C. Schulzke, Temperature dependent electrochemical investigations of molybdenum and tungsten oxobisdithiolene complexes. Dalton Trans., 2005(004), p. 713-720. http://dx.doi.org/10.1039/B414853C.

 

117.     Z. Yang, X. Ma, R. B. Oswald, H. W. Roesky, H. Zhu, C. Schulzke, K. Starke, M. Baldus, H.-G. Schmidt, and M. Noltemeyer, Janus-Faced Aluminum: A Demonstration of Unique Lewis Acid and Lewis Base Behavior of the Aluminum Atom in [LAlB(C6F5)3]. Angew. Chem., 2005, 117(43), p. 7234-7236. http://dx.doi.org/10.1002/ange.200502251.

 

118.     U. Christmann, H. Dau, M. Haumann, E. Kiss, P. Liebisch, D. Rehder, G. Santoni, and C. Schulzke, Substrate binding to vanadate-dependent bromoperoxidase from Ascophyllum nodosum: A vanadium K-edge XAS approach. Dalton Trans., 2004(16), p. 2534-2540. http://pubs.rsc.org/en/Content/ArticleLanding/2004/DT/b405764c.

 

119.     D. Rehder, G. Santoni, G. M. Licini, C. Schulzke, and B. Meier, The medicinal and catalytic potential of model complexes of vanadate-dependent haloperoxidases. Coord. Chem. Rev., 2003, 237(1-2), p. 53-63. http://www.sciencedirect.com/science/article/pii/S0010854502003004.

 

120.     C. Schulzke, D. Enright, H. Sugiyama, G. LeBlanc, S. Gambarotta, G. P. A. Yap, L. K. Thompson, D. R. Wilson, and R. Duchateau, The Unusual Stability of Homoleptic Di- and Tetravalent Chromium Alkyls. Organometallics, 2002, 21(18), p. 3810-3816. http://pubs.acs.org/doi/abs/10.1021/om020237z.

 

121.     Mannar R. Maurya, S. Khurana, C. Schulzke, and D. Rehder, Dioxo- and Oxovanadium(V) Complexes of Biomimetic Hydrazone ONO Donor Ligands: Synthesis, Characterisation, and Reactivity. Eur. J. Inorg. Chem., 2001, 2001(3), p. 779-788. http://onlinelibrary.wiley.com/doi/10.1002/1099-0682%28200103%292001:3%3C779::AID-EJIC779%3E3.0.CO;2-%23/pdf.

 

122.     D. Wang, M. Ebel, C. Schulzke, C. Grüning, Saroj K. S. Hazari, and D. Rehder, Vanadium(IV and V) Complexes Containing SNO (Dithiocarbonylhydrazone; Thiosemicarbazone) Donor Sets. Eur. J. Inorg. Chem., 2001, 2001(4), p. 935-942. http://onlinelibrary.wiley.com/doi/10.1002/1099-0682%28200104%292001:4%3C935::AID-EJIC935%3E3.0.CO;2-J/abstract.

 

123.     R. Hedelt, C. Schulzke, and D. Rehder, A cyanohydridoborato-vanadium(II) complex, trans- V (NCBH3)(2)(thf)(4). Inorg. Chem. Commun., 2000, 3(6), p. 300-302. http://www.sciencedirect.com/science/article/pii/S1387700300000691.

 

124.     D. Rehder, C. Schulzke, H. Dau, C. Meinke, J. Hanss, and M. Epple, Water and bromide in the active center of vanadate-dependent haloperoxidases. J. Inorg. Biochem., 2000, 80(1-2), p. 115-121. http://www.sciencedirect.com/science/article/pii/S0162013400000477.

 

125.     H. Dau, J. Dittmer, M. Epple, J. Hanss, E. Kiss, D. Rehder, C. Schulzke, and H. Vilter, Bromine K-edge EXAFS studies of bromide binding to bromoperoxidase from Ascophyllum nodosum. FEBS Lett., 1999, 457(2), p. 237-240. http://www.sciencedirect.com/science/article/pii/S0014579399010455.

 

126.     M. Bashirpoor, H. Schmidt, C. Schulzke, and D. Rehder, Models for Vanadate-Dependent Haloperoxidases: Vanadium Complexes with O4N-Donor Sets. Chem. Ber., 1997, 130(5), p. 651-657. http://onlinelibrary.wiley.com/doi/10.1002/cber.19971300517/pdf.

 

127.     D. Rodewald, C. Schulzke, and D. Rehder, Alkyne-niobium(I) complexes with functionalized alkynes: synthesis, structure and reactivity. J. Organomet. Chem., 1995, 498(1), p. 29-35. http://www.sciencedirect.com/science/article/pii/0022328X95054939.

 

Book Chapters and Books

128.     A. V. Ardhapure, A. Gholap, C. Schulzke, D. Maiti, and A. R. Kapdi, Chapter 2 - Stille Cross-Coupling Reaction: Early Years to the Current State of the Art. in Palladium-Catalyzed Modification of Nucleosides, Nucleotides and Oligonucleotides; A.R. Kapdi, D. Maiti, and Y.S. Sanghvi, Eds., Elsevier: 2018; p 19-36. DOI: https://doi.org/10.1016/B978-0-12-811292-2.00002-7.https://doi.org/10.1016/B978-0-12-811292-2.00002-7.

 

129.     R. Hille, C. Schulzke, and M. L. Kirk, Molybdenum and Tungsten Enzymes: Bioinorganic Chemistry. Metallobiology 2016: The Royal Society of Chemistry. 241. DOI: 10.1039/9781782628828.10.1039/9781782628828.

 

130.     R. Hille, C. Schulzke, and M. L. Kirk, Molybdenum and Tungsten Enzymes: Biochemistry. Metallobiology 2016: The Royal Society of Chemistry. 348. DOI: 10.1039/9781782623915.10.1039/9781782623915.

 

131.     R. Hille, C. Schulzke, and M. L. Kirk, Molybdenum and Tungsten Enzymes: Spectroscopic and Theoretical Investigations. Metallobiology 2016: The Royal Society of Chemistry. 326. DOI: 10.1039/9781782628842.10.1039/9781782628842.

 

132.     C. Schulzke, An Overview of the Synthetic Strategies, Reaction Mechanisms and Kinetics of Model Compounds Relevant to Molybdenum- and Tungsten-Containing Enzymes. in Molybdenum and Tungsten Enzymes: Bioinorganic Chemistry; R. Hille, C. Schulzke, and M.L. Kirk, Eds., Royal Soc Chemistry: Cambridge, 2016; p 1-7. 

 

133.     C. Schulzke and A. C. Ghosh, Molybdenum and Tungsten Oxidoreductase Models. in Bioinspired Catalysis; W. Weigand and P. Schollhammer, Eds., Wiley-VCH Verlag GmbH & Co. KGaA: 2014; p 349-382. DOI: 10.1002/9783527664160.ch13.10.1002/9783527664160.ch13.

 

134.     C. Schulzke, Molybdenum- and Tungsten-Mediated Oxidations. in Comprehensive Inorganic Chemistry II; J. Reedijk and K. Poeppelmeier, Eds., Elsevier: Oxford, 2013; p 569-591. 

 

135.     C. Schulzke and P. P. Samuel, Molybdenum and Tungsten Cofactor Model Chemistry 2011, New York: Nova Science Publishers Inc. 64. https://www.novapublishers.com/catalog/product_info.php?products_id=14119

 

136.     P. P. Samuel and C. Schulzke, Molybdenum and Tungsten Cofactor Model Chemistry: Past, Present and Future. in Handbook of Inorganic Chemistry Research; D.A. Morrison, Ed. Nova Science Publishers Inc: New York, 2011; p., https://www.novapublishers.com/catalog/product_info.php?products_id=13871

 

137.     C. Schulzke, Bioinorganic electrochemistry. in Spectrosc. Prop. Inorg. Organomet. Compd.; J. Yarwood, R. Douthwaite, and S.B. Duckett, Eds., The Royal Society of Chemistry: 2010; p 111-124. http://pubs.rsc.org/en/Content/Chapter/9781849730853-00111/978-1-84973-085-3

 

Articles without peer review

138.     C. Schulzke, BY DIETER REHDER Bioinorganic vanadium chemistry John Wiley & Sons/Wiley-Blackwell, 2008, 224 pp. (paperback), (hardcover) ISBN 978-0-470-06516-7, 978-0-470-06509-9. Appl. Organomet. Chem., 2009, 23(10), p. 425-426. http://onlinelibrary.wiley.com/doi/10.1002/aoc.1523/abstract.

 

139.     J. Beckmann, R. Pietschnig, S. Rau, and C. a. Schulzke, Anorganische Chemie 2008. Nachrichten aus der Chemie, 2009, 57(3), p. 221-231. http://onlinelibrary.wiley.com/doi/10.1002/nadc.200960573/pdf.

 

140.     C. Schulzke, Bioanorganische Chemie. Nachrichten aus der Chemie, 2008, 56(3), p. 253-257. http://dx.doi.org/10.1002/nadc.200855337.

 

141.     C. Schulzke, Bioanorganische Chemie. Nachrichten aus der Chemie, 2007, 55(3), p. 239-242. http://onlinelibrary.wiley.com/doi/10.1002/nadc.200743606/abstract.

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