Arbeitsgruppe Hartung

Publications from 1996 to 1999

[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, Synthesis 1997,

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, Synlett 1997, 848–850. 

 

 

 

[29] A New and Convenient Access to N-Alkoxypyridine-2(1H)-thiones. J. Hartung, Synlett 1996, 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.

 

 

© AK Hartung

März 2009

 

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