TY - JOUR A1 - Benassi, Rois A1 - Bertarini, C. A1 - Hilfert, Liane A1 - Kempter, Gerhard A1 - Kleinpeter, Erich A1 - Spindler, Jürgen A1 - Taddei, F. A1 - Thomas, Steffen T1 - Exocyclic push-pull conjugated compounds : Part 3 Y1 - 2000 ER - TY - JOUR A1 - Griel, C. A1 - Ströhl, D. A1 - Jeschkeit, H. A1 - Kleinpeter, Erich T1 - Synthetische und NMR-spektroskopische Untersuchungen der Benzzyl-aminaddition an N-Maleyl- aminosäurederivaten Y1 - 1992 ER - TY - JOUR A1 - Kihampa, Charles A1 - Nkunya, Mayunga H. H. A1 - Joseph, Cosam C. A1 - Magesa, Stephen M. A1 - Hassanali, Ahmed A1 - Heydenreich, Matthias A1 - Kleinpeter, Erich T1 - Anti-mosquito and antimicrobial nor-halimanoids, isocoumarins and an anilinoid from Tessmannia densiflora N2 - The nor-halimane diterpenoid tessmannic acid and its methyl, 2-methylisopropyl and 1-methylbutyl esters, the unusual isocoumarins 8-hydroxy-6-methoxy-3-pentylisocoumarin and 7-chloro-8-hydroxy-6-methoxy-3-pentylisocoumarin, and 5- pentyl-3-methoxy-N-butylaniline were isolated from the stem and root bark extracts of Tessmannia densiflora Harms (Caesalpiniaceae) that showed mosquito larvicidal activity. The structures were determined on interpretation of spectroscopic data. Tessmannic acid and its methyl ester exhibited antibacterial and antifungal activity. The compounds also caused high larvae and adult Anopheles gambiae mosquitoe mortality effects, and stronger mosquito repellency than that shown by the standard repellent DEET, hence indicating Tessmannia species to be potential sources of bioactive natural products. Y1 - 2009 UR - http://www.sciencedirect.com/science/journal/00319422 U6 - https://doi.org/10.1016/j.phytochem.2009.07.024 SN - 0031-9422 ER - TY - JOUR A1 - Kihampa, Charles A1 - Joseph, Cosam C. A1 - Nkunya, Mayunga H. H. A1 - Magesa, Stephen M. T1 - Larvicidal and IGR activity of extract of Tanzanian plants against malaria vector mosquitoes N2 - Background & objectives: This paper reports the larvicidal activity of seventeen Tanzanian plant species against the malaria vector, Anopheles gambiae s.s. Giles larvae. Some of the plants are used traditionally as sources of insecticidal materials. Methods: The crude extracts from the leaves, stem and root barks of the investigated plants were obtained by solvent extraction and then bio-assayed following WHO protocols showed LC50 values 10 to 400 ppm after 24 h exposure. The structures were determined on interpretation of spectroscopic data. Results: The most active extracts were those from the stem and root barks of Annona squamosa, Uvaria faulknerae, U. kirkii and Uvariodendron pycnophyllum, all of which had LC50 values between 10 and 100 ppm. Long-term exposure beyond 24 h also showed more susceptibility of the larvae to the extracts. Larvae deformities by forming tail-like structures were observed for the methanol extracts of Tessmannia martiniana var pauloi. Interpretation & conclusion: The results suggest that the investigated plant extracts are promising as larvicides against An. gambiae s.s. Giles mosquitoes and could be useful leads in the search for new and biodegradable plant derived larvicide products. Y1 - 2009 UR - http://www.mrcindia.org/journal/ SN - 0972-9062 ER - TY - JOUR A1 - Ryppa, C. A1 - Senge, Mathias O. A1 - Hatscher, S. S. A1 - Kleinpeter, Erich A1 - Wacker, Philipp A1 - Schilde, Uwe A1 - Wiehe, A. T1 - Synthesis of mono- and disubstituted porphyrins : A- and 5,10-A(2)-type systems N2 - General syntheses have been developed for meso-substituted porphyrins with one or two substituents in the 5,10- positions and no beta substituents. 5-Substituted porphyrins with only one meso substituent are easily prepared by an acid-catalyzed condensation of dipyrromethane, pyrrole-2-carbaldehyde. and an appropriate aldehyde using a "[2+1+1]" approach. Similarly, 5,10-disubstituted porphyrins are accessible by simple condensation of unsubstituted tripyrrane with pyrrole and various aldehydes using a "[3+1]" approach. The yields for these reactions are low to moderate and additional formation of either di- or mono-substituted porphyrins due to scrambling of the intermediates is observed. However, the reactions can be performed quite easily and the desired target compounds are easily removed due to large differences in solubility. A complementary and more selective synthesis involves the use of organolithium reagents for SNAr reactions. Reaction of in situ generated porphyrin (porphine) with 1.1-8 equivalents of RLi gave the monosubstituted porphyrins, while reaction with 3-6 equivalents of RLi gave the 5,10-disubstituted porphyrins in yields ranging from 43 to 90%. These hitherto almost inaccessible compounds complete the series of different homologues of A-, 5,15-A(2)-, 5,10-A(2)-, A(3)-, and A(4)-type porphyrin's and allow an investigation of the gradual influence of type, number, and regiochemical arrangement of substituents on the properties of meso-substituted porphyrins. They also present important starting materials for the synthesis of ABCD porphyrins and are potential synthons for supramolecular materials requiring specific substituent orientations Y1 - 2005 SN - 0947-6539 ER - TY - JOUR A1 - Balci, K. A1 - Akkaya, Y. A1 - Akyuz, S. A1 - Collier, W. B. A1 - Stricker, M. C. A1 - Stover, D. D. A1 - Ritzhaupt, G. A1 - Koch, Andreas A1 - Kleinpeter, Erich T1 - The effects of conformation and zwitterionic tautomerism on the structural and vibrational spectral data of anserine JF - Vibrational spectroscopy : an international journal devoted to applications of infrared and raman spectroscopy N2 - In this study, the stable conformers of neutral anserine were searched by molecular dynamics simulations and energy minimization calculations using the MM2 force field. Thermochemical calculations at B3LYP/6-31G(d) level of theory followed these preliminary calculations. The results confirmed that neutral anserine has quite a flexible structure and many stable gauche and trans conformers at room temperature. Nevertheless, two are considerably more favourable in energy than the others and expected to dominate the gas-phase and matrix IR spectra of the molecule. The corresponding structural and vibrational spectral data for these two conformers of neutral anserine, whose relative stabilities were also examined by high-accuracy energy calculations carried out using G3MP2B3 method, and for the most stable conformer of anserine in zwitterion form were calculated at B3LYP/6-311++G(d,p) level of theory. The calculated harmonic force constants were refined using the Scaled Quantum Mechanical Force Field (SQM-FF) method and then used to produce the refined wavenumbers, potential energy distributions (PEDs) and IR and Raman intensities. These refined data together with the scaled harmonic wavenumbers obtained using another method, Dual Scale factors (DS), enabled us to correctly analyse the observed IR and Raman spectra of anserine and revealed the effects of conformation and zwitterionic tautomerism on its structural and vibrational spectral data. (C) 2016 Elsevier B.V. All rights reserved. KW - Anserine KW - Matrix IR spectrum KW - Tautomerism KW - SQM-FF KW - Dual scale factors Y1 - 2016 U6 - https://doi.org/10.1016/j.vibspec.2016.08.003 SN - 0924-2031 SN - 1873-3697 VL - 86 SP - 277 EP - 289 PB - Elsevier CY - Amsterdam ER - TY - JOUR A1 - Kleinpeter, Erich A1 - Koch, Andreas A1 - Fischer, G. A1 - Askolin, C.-P. T1 - 13 C NMR, 15 N NMR and quantum-chemical study of the tautomerism of 2-substituted 5-ME-7-OH-1,2,4-triazolo[1,5- a]pyrimidines Y1 - 1997 ER -