[40] Molecular Basis, Pharmacology and Physiological Role of Cardiac KATP  Channels. H. Gögelein, J. Hartung, H.C. Englert,Cell Physiol. Biochem. 1999, 9, 227–241.

[39] Die Biosynthese von Barbamid – ein neuer radikalischer Weg zur ”Biohalogenierung”? J. Hartung, Angew. Chem.1999, 111, 1287–1289;
Angew. Chem., Int. Ed. Engl. 1999, 38, 1209–1211.

[38] A New Generation of Alkoxyl Radical Precursors – Preparation and Properties of N-(Alkoxy)-4-arylthiazole-2(3H)-thiones. J. Hartung, M. Schwarz, I. Svoboda,
H. Fueß, M.-T. Duarte, Eur. J. Org. Chem.1999, 1275–1290.

[37] On Selective O-Alkylation of Ambident Nucleophiles – The Synthesis of Thiohydroxamic Acid O-Esters via Phase Transfer Reactions. J. Hartung, R. Kneuer,
M. Schwarz, I. Svoboda, H. Fueß, Eur. J. Org. Chem.1999, 97–106.

[36] H 1883, a novel cardioselective inhibitor of the ATP-sensitive potassium channel. Part I: Effects on cardiomyocytes, coronary flow and pancreatic beta-cells.
H. Gögelein, J. Hartung, H.C. Englert, B.A. Schölkens,J. Pharmacol. Exp. Ther.1998, 286, 1456–1464.

[35] The Crystal Structure of S-(2-phenyl-4-penten-1-yl)-2-thiopyridine N-oxide (C₁₆H₁₇NOS). J. Hartung, I. Svoboda, H. Fuess, Z. Kristallogr. 1998, 213, 319–320.

[34] Transition Metal Peroxo Complexes as Versatile Tools in the Oxidative Ring Closure of Substituted 4-Pentenols – The Synthesis of Tetrahydrofurans and
Tetrahydropyrans. J. Hartung, P. Schmidt in: Selective Reactions of Metal-activated Molecules (Hrsg.: H. Werner,  P. Schreier), Vieweg, Braunschweig, 1998, 65–69.

[33] 1,4-Diazabicyclo[2.2.2]octane (DABCO) – an Efficient Reagent in the Synthesis of Alkyl Tosylates or Sulfenates. J. Hartung, S. Hünig, R. Kneuer,
M. Schwarz, H. Wenner, Synthesis1997, 1433–1438.

[32] A Network of Hydrogen Bonds. The Packing and the Molecular Geometry of 1-Hydroxy-4(1H)-pyridinethione in the Solid State. J. Hartung, I. Svoboda,
H. Fuess, M.–T. Duarte, Acta Cryst. 1997, C53, 1631–1634.

[31] Lone Pair Repulsion in Cyclic Hydroxamic Acid O-Esters. The Structure of N-Cyclohexyloxy-2(1H)-pyridone. J. Hartung, I. Svoboda, H. Fuess, M.-T. Duarte,
Acta Cryst. 1997, C53, 1629–1631.

[30] Towards Improved Alkoxyl Radical Precursors – The Synthesis of N-Alkoxy-4-(p-chloro-phenyl)thiazole-2(3H)-thiones. J. Hartung, M. Schwarz, Synlett1997, 848–850. 

[29] A New and Convenient Access to N-Alkoxypyridine-2(1H)-thiones. J. Hartung, Synlett1996, 1206-1209.

[28] 5-Exo or 6-endo ? Exploring Transition State Geometries of 4-Penten-1-oxyl Radical Ring Closures. J. Hartung, R. Stowasser, D. Vitt, G. Bringmann,
Angew. Chem.1996, 108, 3056-3059, Angew. Chem. Int. Ed. Engl.1996, 35, 2820–2823.

[27] Solid State and Solution Structures of O-Alkyl- and of O-Acyl Derivatives of 1-Hydroxypyridine-2(1H)-thione. J. Hartung, M. Hiller, M. Schwarz,
I. Svoboda, H. Fuess, Liebigs Ann. 1996, 2091–2097.

[26] Balancing Conjugational Stabilization and Steric Strain. The Solid State Geometry of a 2-Thioalkyl-subsituted Pyridine N-Oxide. J. Hartung,
I. Svoboda, H. Fuess, Acta Cryst. 1996, C52, 2841–2844.

[25] Exploring Transition State Geometries of 4-Penten-1-oxyl and 5-Hexen-1-yl Radical Ring Closures by ab initio Computational Methods. J. Hartung,
R. Stowasser, D. Vitt, G. Bringmann in Overview of Research Projects on the CRAY Y-MP at the Leibnitz-Rechenzentrum München (Hrsg.: C. Schaller, M. Brehm),
Bayerische Akademie der Wissenschaften, München, 1996, Bericht 9601, S. 157–160.

[24] Polar and Steric Substituent Effects in 5-exo-trig Cyclizations of 1-Aryl-4-penten-1-oxyl Radicals. J. Hartung, M. Hiller, P. Schmidt, Liebigs Ann.1996, 1425–1436.

[23] Photoreactions of Phenyl Substituted N-(4-Pentenyl-1-oxy) pyridine-2-(1H)-thiones. J. Hartung, M. Hiller, P. Schmidt, Chem. Eur. J.1996, 2, 1014–1023