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Publications

39) "Enantioselective Preparation of 3-Arylcycloalkylamines by Rhodium-Catalyzed 1,4-Addition and Subsequent Stereodivergent Reduction"

S. Gebhardt, C. H. Müller, J. Westmeier, K. Harms, P. von Zezschwitz, Adv. Synth. Catal. 2015, 357, 507-514.

 

38) "Copper-Catalyzed Enantioselective 1,4-Addition of Alkyl Groups to N-Sulfonyl Imines"

J. Westmeier, P. von Zezschwitz, Chem. Commun. 2014, 50, 15897-15900.

Highlighted: "Asymmetric 1,4-Addition of Alkyl Groups to N-Sulfonyl Imines"

H. Yamamoto, S. Bhadra, Synfacts 2014, 10, 1277.

 

37) "Rhodium-Catalyzed Enantioselective Addition of Organoaluminum Reagents to N-Tosyl Ketimines" 

S. Hirner, A. Kolb, J. Westmeier, S. Gebhardt, S. Middel, K. Harms, P. von Zezschwitz, Org. Lett. 2014, 16, 3162-3165.

Highlighted: "Rhodium-Catalyzed Asymmetric Addition to Ketimines"

H. Yamamoto, M. Sai, Synfacts 2014, 10, 837.

 

36) "Convenient Access to Cycloalk-2-enone-Derived N-Sulfonyl Imines"

S. Hirner, J. Westmeier, S. Gebhardt, C. H. Müller, P. von Zezschwitz, Synlett 2014, 25, 1697-1700.

 

35) "Improved Synthesis of Cyclic Tertiary Allylic Alcohols by Asymmetric 1,2-Addition of AlMe3 to Enones"

A. Kolb, W. Zuo, J. Siewert, K. Harms, P. von Zezschwitz, Chem. Eur. J. 2013, 19, 16366-16373.

 

34) "Total Synthesis of (R)-Sarkomycin via Asymmetric Rhodium-catalyzed Conjugate Addition"

J. Westmeier, S. Kress, C. Pfaff, P. von Zezschwitz, J. Org. Chem. 2013, 78, 10718-10723.

33) "First Tandem Asymmetric Conjugate Addition of Alkenyl Nucleophiles and Silyl Trapping of the Intermediate Enolates"

J. Westmeier, C. Pfaff, J. Siewert, P. von Zezschwitz, Adv. Synth. Catal. 2013, 355, 2651-2658.

32) "Enantioselective Synthesis of 3,4-Disubstituted cis- and trans-1,2,5-Thiadiazolidine-1,1-dioxides as Precursors for Chiral 1,2-Diamines"

C. Schüttler, Z. Li-Böhmer, K. Harms, P. von Zezschwitz, Org. Lett. 2013, 15, 800-803.

Highlighted: "Enantioselective Synthesis of cis- and trans-Thiazolidines"

M. Lautens, J. Tsoung, Synfacts 2013, 9, 511.

 

31) "Organoaluminum Couplings to Carbonyls, Imines, and Halides"

A. Kolb, P. von Zezschwitz, Top. Organomet. Chem. 2013, 41, 245-276.

 

30) "The Binding Site of the V-ATPase Inhibitor Apicularen Is in the Vicinity of Those for Bafilomycin and Archazolid"

C. Osteresch, T. Bender, S. Grond, P. von Zezschwitz, B. Kunze, R. Jansen, M. Huss, H. Wieczorek, J. Biol. Chem. 2012, 287, 31866-31876.

 

29) "Kinetic Resolution of Chiral Cyclohex-2-enones by Rhodium(I)/binap-Catalyzed 1,2- and 1,4-Additions"

A. Kolb, S. Hirner, K. Harms, P. von Zezschwitz, Org. Lett. 2012, 14, 1978-1981.

 

28) "Archazolid A Binds to the Equatorial Region of the c-Ring of the Vacuolar H+-ATPase"

S. Bockelmann, D. Menche, S. Rudolph, T. Bender, S. Grond, P. von Zezschwitz, S.P. Muench, H. Wieczorek, M. Huss, J. Biol. Chem. 2010, 285, 38304-38314.

 

27) "New Fluorous Photoaffinity Labels (F-PAL) and Their Application in V-ATPase Inhibition Studies"

N. Burkard, T. Bender, J. Westmeier, C. Nordmann, M. Huss, H. Wieczorek, S. Grond, P. von Zezschwitz, Eur. J. Org. Chem. 2010, 11, 2176-2181.

 

26) "Total Synthesis of 4-Acetyl-1,3-dihydroimidazo[4,5-c]pyridin-2-one, a New Microbial Metabolite from a Streptomyces Species"

T. Bender, P. von Zezschwitz, Nat. Prod. Commun. 2009, 4, 971-976.

25) “Neues von einem alten Bekannten”

P. von Zezschwitz, Nachr. Chem. 2008, 56, 1141–1144.

 

24) ”The New Metabolite (S)-Cinnamoylphosphoramide from Streptomyces sp. and its Total Synthesis“

M. Quitschau, T. Schuhmann, J. Piel, P. von Zezschwitz, S. Grond, Eur. J. Org. Chem. 2008, 5117–5124.

 

23) “Aminierungen: die C-H-Bindung als funktionelle Gruppe”

P. von Zezschwitz, Nachr. Chem. 2008, 56, 897–901.

 

22) “Organokatalyse durch asymmetrische Protonierung?”

P. von Zezschwitz, Nachr. Chem. 2008, 56, 764–767.

 

21) “ATPase-Inhibitoren Archazolid und Cruentaren: Totalsynthesen”

P. von Zezschwitz, Nachr. Chem. 2008, 56, 535–540.

 

20) “Selectivity Control in 1,2- and 1,4-Additions of Aluminium Organyls to Carbonyl Com­pounds”

P. von Zezschwitz, Synthesis 2008, 1809–1831.

 

19) “Gratwanderung zwischen Reaktivität und Selektivität”

P. von Zezschwitz, Nachr. Chem. 2008, 56, 38–41.

 

18) “Iromycins from Streptomyces sp. and from Synthesis: New Inhibitors of the Mitochondrial Electron Transport Chain“

F. Surup, H. Shojaei, P. von Zezschwitz, B. Kunze, S. Grond, Bioorg. Med. Chem. 2008, 16, 1738–1746.

 

17) “Rhodium-Catalyzed Enantio­selec­tive 1,2-Addition of Aluminum Organyls to Cyclic Enones“

J. Siewert, R. Sandmann, P. von Zezschwitz, Angew. Chem. 2007, 119, 7252–7254; Angew. Chem. Int. Ed. 2007, 46, 7122–7124.

 

16) “Iromycins: A New Family of Pyridone Metabolites from Streptomyces sp. II. Convergent Total Synthesis“

H. Shojaei, Z. Li-Böhmer, P. von Zezschwitz, J. Org. Chem. 2007, 72, 5091–5097.

 

15) ”Convenient Synthesis of a [1‑14C]Diazirinylbenzoic Acid as a Photoaffinity Label for Binding Studies of V-ATPase Inhibitors“

T. Bender, M. Huss, H. Wieczorek, S. Grond, P. von Zezschwitz, Eur. J. Org. Chem. 2007, 3870–3878.

 

14) “Spirodionic Acid, a Novel Meta­bo­li­te from Streptomyces sp., Part II: Total Synthesis through a Twofold Michael Addition as a Selec­tive Spiroannelation Strategy”

J. Siewert, A. Textor, S. Grond, P. von Zezschwitz, Chem. Eur. J. 2007, 13, 7424–7431.

 

13) “Spirodionic Acid, a Novel Metabolite from Strepto­myces, Part I: Struc­ture Elucidation and Diels-Alder-Type Biosynthesis”

A. Textor, I. Papastavrou, J. Siewert, J. Magull, A. Kulik, H.-P. Fiedler, P. von Zez­schwitz, S. Grond, Chem. Eur. J. 2007, 13, 7416–7423.

 

12) “A Com­pre­hen­sive Study of Okaspirodiol: Characterization, Total Synthesis and Biosynthesis of a New Meta­bolite from Streptomyces sp.”

T. Bender, T. Schuhmann, J. Magul, S. Grond, P. von Zezschwitz, J. Org. Chem. 2006, 71, 7125–7132.

 

11) “Domino Heck-Pericyclic Reactions“

P. von Zezschwitz, A. de Meijere, Top. Orga­no­met. Chem. 2006, 19, 49–89.

 

10) The Virtue of Palladium-Catalyzed Domino Reactions – Diverse Oligocycli­za­tions of Acyclic 2-Bromoenynes and 2-Bro­mo­enedi­ynes”

A. de Meijere, P. von Zezschwitz, S. Bräse, Acc. Chem. Res. 2005, 38, 413–422.

 

9) “A New Photo­trans­formation of Methoxycarbonyl-Substituted (E,Z,E)-1,3,5-Hexatrienes: Easy Access to Ring-Annelated 8-Oxabicyclo[3.2.1]octa-2,6-diene Derivatives”

R. von Essen, P. von Zezschwitz, D. Vidovic, A. de Meijere, Chem. Eur. J. 2004, 10, 4341–4352.

 

8) “New Cascade and Multiple Cross-Coupling Reactions for the Efficient Construction of Complex Molecules”

A. de Meijere, P. von Zezschwitz, H. Nüske, B. Stulgies, J. Organomet. Chem. 2002, 653, 129–140.

 

7) “A One-Pot Sequence of Stille and Heck Couplings: Synthesis of Various 1,3,5-Hexa­tri­enes and Their Subsequent 6Π-Electro­cycliza­tions”

P. von Zezschwitz, F. Petry, A. de Meijere, Chem. Eur. J. 2001, 7, 4035–4046.

 

6) “A New Methodology for Ring Enlargements by the Oxy-Cope Rearrangement: Ready Access to Highly Functionalized Medium-Size Rings”

P. von Zezschwitz, K. Voigt, M. Noltemeyer, A. de Meijere, Synthesis 2000, 1327–1340.

 

5) “Palladium-katalysierte Kreuzkupplungen zu 1,2-Dialkenyl­cyclo­alkenen: Aus­gangs­stoffe zur Synthese vielfältiger cyclischer Kohlenstoffgerüste“

P. von Zezschwitz, Dissertation, Universität Göttingen, 1999.

 

4) “Versatile Synthesis of 11-Oxabicyclo[4.4.1]undeca-1,5-dienes by Selective Epoxi­dation of 1,6-Disubstituted (E,Z,E)-1,3,5-Hexatrienes and Subsequent Cope Rearrangement”

P. von Zezschwitz, K. Voigt, A. Lansky, M. Noltemeyer, A. de Meijere, J. Org. Chem. 1999, 64, 3806–3812.

 

3) “The Twofold Heck Reaction on 1,2-Dihalocycloalkenes and Subsequent 6Π-Elec­tro­­cycliza­tion of the Resulting (E,Z,E)-1,3,5-Hexatrienes: A New Formal {2+2+2}-Assembly of Six-Membered Rings”

K. Voigt, P. von Zezschwitz, K. Rosauer, A. Lansky, A. Adams, O. Reiser, A. de Mei­jere, Eur. J. Org. Chem. 1998, 1521–1534.

 

2) “Asymmetrische Alkensynthesen durch kinetische Racematspaltungen von Alde­hyden mit chiralen Phosphonaten“

R. Kreuder, K. Bodmann, P. von Zezschwitz, J. Anvelt, A. Soone, T. Rein, O. Reiser in Chemie nachwachsender Rohstoffe, Bundesministerium für Umwelt, Ju­gend und Familie (Hrsg.), Wien 1998, 25–29.

 

1) “Erste dynamische kine­tische Enantiomerentrennung von α-Aminoalde­hy­den“

T. Rein, R. Kreuder , P. von Zezschwitz, C. Wulff, O. Reiser, Angew. Chem. 1995, 107, 1099–1102; Angew. Chem. Int. Ed. Engl. 1995, 34, 1023–1025.