1. Isolierung, Synthese und absolute Konfiguration von Filberton, dem aktiven Prinzip des Haselnußaromas.

Johann Jauch, Dieter Schmalzing, Volker Schurig, Roland Emberger, Rudolf Hopp, Manfred Köpsel, Wilhelm Silberzahn und Peter Werkhoff, Angew. Chem. 101, 1039 (1989).

2. Analysis of the Chiral Aroma Compound Filbertone by Inclusion Gas Chromatography.

Volker Schurig, Johann Jauch, Dieter Schmalzing, Martin Jung, Wilfried Bretschneider, Rudolf Hopp and Peter Werkhoff, Z. Lebensm. Unters. Forsch. 191, 28 (1990).

3. Enantiomeric Composition of Filbertone in Hazelnuts in Relation to Extraction Conditions. Multidimensional GC and GC-MS (SIM) of a Natural Sample.

Gracia P. Blanch, Johann Jauch, J. Agric. Food Chem. 46, 4283-4286 (1998).

4. Improved Synthesis of (S)-Filbertone.

Johann Jauch, Harri Czesla, Volker Schurig, Tetrahedron 55, 9787-9792 (1999).

Modellverbindungen für Azadirachtin

1. Structure of the dimer of racemic exo-3-hydroxy-bicyclo [2.2.1] hepten-2-one.

Johann Jauch, Volker Schurig and Leonhard Walz, Z. Kristallographie 196, 255 (1991).

2. An Improved Procedure for the Preparation of Substituted 4-Hydroxy-4,5-dihydrofurans.

Johann Jauch and Volker Schurig, Tetrahedron Lett. 32, 4687-4690 (1991).

3. Structure of [1R-(endo, anti)]-3-Bromo-1,7-dimethyl-7-vinylbicyclo[2.2.1] heptan-2-one.

Johann Jauch, Heinz Laderer and Leonhard Walz, Acta Cryst. C48, 1246 (1992).

4. Synthesis and Stereochemistry of Bicyclic a-Hydroxy-ketones.

Johann Jauch, Tetrahedron 50, 12903-12912 (1994).


1. Synthesis of Chiral Calix[n]arenes - I. A Synthetic Approach Towards a New Enantiomerically Pure Calix[8]arene Drivative.

Johann Jauch and Volker Schurig, Tetrahedron: Asymmetry 8, 169-172 (1997).

2. Synthesis of Chiral Calix[n]arenes - II. Synthesis of New Chiral Calix[n]arenes based on p-Hydroxy-phenyl-menthone.

Antonio Soi, Jens Pfeiffer, Johann Jauch, Volker Schurig, Tetrahedron: Asymmetry 10, 177-182(1999).

3. Synthesis of New Terpene-derived Phenols, Stereochemistry of 6-(4'-Hydroxyphenyl)-1,6-dihydrocarvone.

J. Pfeiffer, J. Jauch, V. Schurig, Enantiomer 4, 363-368 (1999).

4. Gas Chromatographic Studies employing p-(2'-Methyltridecyl-2')-calix[8]arene Diluted in Polysiloxane as Stationary Phase.

B. Gross, J. Jauch, V. Schurig, J. Microcol. Sep. 11, 313-317 (1999).

Mniopetale und Kuehneromycine

1. A New Protocol for Baylis-Hillman-Reactions: Chirality Transfer in a Lithium Phenylselenid induced Tandem-Michael-Aldol-Retro-Michael-Reaction.

Johann Jauch, J. Org. Chem. 66, 609-611 (2001).

2. Improved Synthesis of 3-Bromo-2,2-dimethyl-propanal, a Versatile Building Block for Compounds with two Geminal Methyl Groups on a Quarternary Center.

Johann Jauch, J. Prakt. Chemie 342, 100-101 (2000).

3. Synthesic Studies towards Mniopetals (I). A Short Synthesis of a Key Intermediate for the Total Synthesis of Mniopetals.

Johann Jauch, Synlett 1999, 1325-1327.

4. A Short Total Synthesis of Kuehneromycin A.

Johann Jauch, Angewandte Chemie 112, 2874-2875 (2000).

5. Intramolecular Diels-Alder Reactions with Substituted Feringa-Butenolides. A Dramatic Increase in Reactivity by Double Activation.

Ulrich Reiser, Johann Jauch, Eberhard Herdtweck, Tetrahedron: Asymmetry 11, 3345-3349 (2000).

6. Synthetic Studies towards Mniopetals (II). A Short and Efficient Synthesis of Mniopetal E.

Johann Jauch, Synlett 2001, 87-89.

7. Synthetic Studies towards Mniopetals (III). Solid Phase Organic Synthesis of a Key Intermediate for Combinatorial Synthesis of Mniopetals, Kuehneromycins and Marasmanes.

Ulrich Reiser, Johann Jauch, Synlett 2001, 90-92.

8. Synthetic Studies towards Mniopetals (IV). A Short Total Synthesis of Mniopetal F.

Johann Jauch, Eur. J. Org. Chem. 2001, 473-476.

9. Arbeiten zur Totalsynthese der Mniopetale, Kuehneromycine und Marasmone in Lösung und an fester Phase.

Johann Jauch, Habilitationsschrift, TU München, 2001.

10. Total Synthesis of Anhydromarasmone

Johann Jauch, Carsten Wallner, Eberhardt Herdtweck, Eur. J. Org. Chem. 2003, 3060-3064.

11. Synthesis of Kuehneromycin B and Panudial from Kuehneromycin A

Carsten Wallner, Johann Jauch, Synthesis 2004, 665-667.

Inhaltsstoffe aus Weihrauch und Myrrhe

1. Ein einfaches Verfahren zur Synthese von Boswelliasäuren und Derivaten davon.

Johann Jauch, PCT-Anmeldung am 1. 3. 2001; Registrier-Nr. PCT/EP 02/02249.

2. An Efficient Method for the Large-Scale Preparation of 3-O-Acetyl-11-oxo-ß-boswellic Acid and other Boswellic Acids

Johann Jauch, Jochen Bergmann, Eur. J. Org. Chem. 4752-4756 (2003)

3. Totalsynthese von Myrtucommulon A

H. Müller, M.  Paul, D. Hartmann, V. Huch, D. Blaesius, A. Koeberle, O. Werz, J. Jauch, Angew. Chem. Int. Ed. Engl. 49, 2045-2049 (2010)

4. Qualitative and Quantitative Analysis of 17 Different Types of Tetra- and Pentacyclic Triterpenic Acids in Boswellia papyrifera by a Semi-Automatic Homomodal 2D HPLC method

Michael Paul, Gerit Brüning, Joachim Weihrather and Johann Jauch; Chromatographia 74, Vol 1-2, 29-40 (2011)

5. A Thin-Layer-Chromatography Method for the Identification of Three Different Olibanum Species (Boswellia papyrifera, Boswellia serrata and Boswellia sacra, respectively, Boswellia carterii)

Michael Paul, Gerit Brüning, Jochen Bergmann and Johann Jauch; Phytochemical Analysis 23, Issue 2, 184-189 (2012)

6. Efficient Preparation of Incensole and Incensole Acetate, and Quantification of These Bioactive Diterpenes in Boswellia papyrifera by a RP-DAD-HPLC Method

Michael Paul and Johann Jauch; Natural Products Communications 7, Issue 3, 283-288 (2012)

Publikationen als Kooperationspartner mit anderen Gruppen

1. Studies on the non-mevalonate isoprenoid biosynthetic pathway. Simple methods for the preparation of isotope-labeled (E)-1-hydroxy-2-methyl-but-2-enyl-4-diphosphate.

Stefan Hecht, Sabine Amslinger, Johann Jauch, Klaus Kis, Viola Trentinaglia, Petra Adam, Wolfgang Eisenreich, Adelbert Bacher, Felix Rohdich, Tetrahedron Lett. 43, 8929-8933 (2002).

 2. Boswellic Acids Stimulate Arachidonic Acid Release and 12-Lipoxygenase Activity in Human Platelets Independent of Ca2+ and Differentially Interact with Platelet-Type 12-Lipoxygenase

Daniel Poeckel, Lars Tausch, Nicole Kather, Johann Jauch, and Oliver Werz, Mol. Pharmacol. 70, 1071-1078 (2006)

3. Boswellic acids interact with cyclooxygenases and inhibit cyclooxygenase activity

Siemoneit, U., Hofmann, B., Kather, N., Franke, L., Schneider, G., Jauch, J., Poeckel, D. and Werz, O., Biochem. Pharmacol. 75, 503-513 (2008)

4. Identification of human cathepsin G as a functional target of boswellic acids from the anti-inflammatory remedy frankincense

L. Tausch, A. Henkel, U. Siemoneit, D. Poeckel, N. Kather, L. Franke, G. Schneider, C. Angioni, G. Geisslinger, C. Skarke, W. Holtmeier, T. Beckhaus, M. Karas, J. Jauch and O. Werz, J. Immunol. 183, 3433-3442 (2009)

5. A new Bacillus megaterium whole-cell catalyst for the hydroxylation of the pentacyclic triterpene 11-keto-β-boswellic acid (KBA) based on a recombinant cytochrome P450 system

Sabrina Bleif, Frank Hannemann, Josef Zapp, David Hartmann, Johann Jauch und Rita Bernhardt, Appl. Microbiol. Biotechnol. 93, 1135-1146 (2012)

6.Are Free Radicals Involved in IspH Catalysis? An EPR and Crystallographic Investigation

Weixue Wang, Ke Wang, Ingrid Span, Johann Jauch, Adelbert Bacher, Michael Groll and Eric Oldfield, J. Am. Chem. Soc. 134 (27), 11225–11234 (2012)