Publications (selection)

·    P. Imming, R. Mohr, E. Müller, W. Overheu, G. Seitz, (4+1)-Cycloaddition von Isocyaniden an 1,2,4,5-Tetrazine: eine neue Pyrazol-Synthese. Angew. Chem. 1982, 94, 291.

·    S. Druecke, P. Imming, T. Kaempchen, G. Seitz, Cross-conjugated polychlorinated derivatives of cycloheptatriene from octachlorocycloheptatriene and hexachlorotropone. Chem. Ber. 1988, 121(9), 1595-600.

  J. E. Baldwin, R. M. Adlington, A. Basak, P. Imming, K. Ponnamperuma, H. Ronneberg, C. J. Schofield, H.-H. Ting, N. J. Turner, Penicillin-Biosynthesis: Active Substrates derived by Methoxy Substitution in the Valinyl Residue of the Natural Substrate. J. Chem. Soc., Chem. Commun. 1989, 802-804.

·    P. Imming, G. Seitz, Synthesis of 3,5-Dihydroxytropone. Chem. Ber. 1989, 122, 2183-2185.

 G. Seitz, P. Imming, Oxocarbons and Pseudooxocarbons. Chem. Rev. 1992, 92, 1227-1260.

·    P. Imming, A. Kuemmell, G. Seitz, Inverse [4+1] cycloadditions of 3-methyl-2,3-dihydro-1,3-benzothiazole-2-ylidene with 1,2,4,5-tetrazines. Heterocycles 1993, 35(1), 299-304.

·    P. Imming, Synthesis of the First Penicillin Derivatives With Medium-Sized Lactam Ring and of Related Thiazolidines. Arch. Pharm. 1995, 328, 207-215.

·    P. Imming, M.-H. Jung,  Pentafluorophenyl esters of dicarboxylic acids. Arch. Pharm. 1995,  328(1),  87-91.

 B. Greve, P. Imming, St. Laufer, Effiziente Synthese neuer 2-Cycloalkylpropansäure-Derivate - Mittlere Ringe als Bioisostere von Alkylphenylresten? Angew. Chem. 1996, 108, 1312-1314 (Angew. Chem. Int. Ed. Engl. 1996, 35, 1221-1223).

·    P. Imming, Künstliche Paradiese. Die Scheinwelt der Drogen und Suchtmittel. Pharmaz. Ztg. 1996, 141, 3635-3645.

·    G. Seitz, P. Imming, Thio- and Seleno-Substituted Cyclobutenediones. S. 951, 983-996 u. 1041-1044 in: HOUBEN/WEYL Methoden der Organischen Chemie, Bd. E 17f, 'Carbocyclic 4-Membered Ring Compounds' (Hg. A. de Meijere), Stuttgart: Thieme Verlag 1997.

·    B. Klar, P. Imming, Asymmetric Induction in the Preparation of Penicillin-Analogous Thiazepines, Liebigs Ann./Recueil 1997, 1711-1718.

 P. Imming, B. Greve, Regioselectivity of Water Elimination as a Function of Ring-Size, J. Org. Chem. 1997, 62, 8058-8062.

·    L. A. Dailey, P. Imming, "12-Lipoxygenase: Classification, Possible Therapeutic Benefits from Inhibition, and Inhibitors." Curr. Medicin. Chem. 1999, 6, 389-398.

·    P. Imming, J. Becker, Ch. Blümer, B. Sauer, B. Schulze, G. Laufenberg, Identification of Tropic Acid in Tropicamide Ph. Eur. 1997. Pharmeuropa 1999, 11, 313-314.

 P. Imming, B. Klar, D. Dix, Hydrolytic Stability vs. Ring Size in Lactams - New Perspectives for the Development of Lactam Antibiotics and other Serine Protease Inhibitors. J. Med. Chem. 2000, 43, 4328-4331.

   Imhof, P. Imming, M. Zentgraf, An improved synthetic procedure for 6,6'-dibromoindigo (Tyrian purple). Synthetic Communications 2001, 31(23), 3721-3727.

  P. Imming, S. Goeters, G. Pawlitzki, B. Hempel, The absolute configuration of guaianolides, matricin and its epimers, and chamazulene carboxylic acid. Chirality 2001, 13, 337-341.

  P. Imming, M. Graf, S. Tries, R. Hirschelmann, E. Krause, G. Pawlitzki, Anti-inflammatory Planar Chiral [2.2]Paracyclophane Acetic Acid Enantiomers. Inflamm. Res. 2001, 50, 371-374.

 Chamazulencarbonsäureverbindungen und deren Verwendung. Ger. Offen. DE 10065683 A1 5 Jul 2001 (Chem. Abstr. 2001, 135, 76647).

·    P. Imming, O. Germershaus, The products of the determination of the iodine value with iodine monobromide. Arch. Pharm. Pharm. Med. Chem. 2002, 335, 449-451.

   T. Hitziger, P. Höll, M. Ramadan, D. Dettmering, P. Imming, B. Hempel, Die alte junge Kamille. Pharmaz. Ztg. 2003, 148, 372-380.

  M. Laemmerhofer; P. Imming; W. Lindner, Direct high-performance liquid chromatographic enantiomer separation of anti-inflammatory planar chiral [2.2]paracyclophane-4-acetic acid. Chromatographia 2004, 60(Suppl. 1),  S13-S17

  P. Imming; T. Buss; L. A. Dailey; A. Meyer; H. Morck; M. Ramadan; T.  Rogosch, A classification of drug substances according to their mechanism of action. Pharmazie 2004, 59(8), 579-589.

A. Meyer, S. Zimmermann, B. Hempel, P. Imming, Anthecotulide: Purification, Analytical Data, Absence from Chamomile Preparations, Stability and Reactivity, and Anti-infective Testing. J. Nat. Prod. 2005, 68(3). 432-434.

·    "Pharmacology and Toxicology", "Active chemical constituents of Chamomilla recutita (L.) Rauschert syn. Matricaria chamomilla L." und "Chemical analysis of the active principles of chamomile" in: Chamomile - Industrial Profiles, Hgg. R. Franke u. H. Schilcher. CRC Press, Boca Raton 2005. Taylor & Francis 2005, ISBN: 0415334632

 M. Ramadan; S. Goeters; B. Watzer; E. Krause; K.  Lohmann; R.  Bauer; B. Hempel; P.  Imming, Chamazulene Carboxylic Acid and Matricin: A Natural Profen and Its Natural Prodrug, Identified through Similarity to Synthetic Drug Substances. J. Nat. Prod. 2006, 69(7), 1041-1045.

  P. Imming, C. Sinning, A. Meyer; Drugs, their targets and the nature and number of drug targets, Nature Reviews Drug Discovery 2006, 5 (10), 821-834. doi:10.1038/nrd2132


            
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