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1

Alan, Jones R., ed. Pyrroles. New York: Wiley, 1990.

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2

1929-, Bean Gerritt Post, ed. The chemistry of pyrroles. London: Academic Press, 1997.

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3

T͡Sveniashvili, V. Sh. Ėlektrokhimii͡a azolov. Tbilisi: "Met͡sniereba", 1990.

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4

Kawamoto, Yusuke. Synthesis and Biological Evaluation of Pyrrole–Imidazole Polyamide Probes for Visualization of Telomeres. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-6912-4.

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5

Dietz, Wolfram Georg. 2,5-Hexandion und Pyrrole im Urin des Menschen: Analytische Bestimmung und Untersuchung der Ausscheidung nach Exposition gegen n-Hexan. Neuherberg: GSF-Forschungszentrum für Umwelt und Gesundheit, 1994.

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6

Scott, Andrew William. Preparation of fluorinated pyrrolo[2,3-d]pyrimidine. Birmingham: University of Birmingham, 1995.

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7

Mwashimba, Paul Guyo. The Birch reduction of electron-deficient pyrroles. Manchester: University of Manchester, 1996.

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8

Voro, Tevita N. Synthesis of potentially biologically active indoles and pyrroles. Norwich: Universityof East Anglia, 1990.

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9

Zirngibl, Ludwig. Antifungal azoles: A comprehensive survey of their structures and properties. Weinheim: Wiley-VCH, 1998.

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10

M, Jordan P., ed. Biosynthesis of tetrapyrroles. Amsterdam: Elsevier, 1991.

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11

Elsadig, Hwaida Misbah. Synthesis of pyrrolo[2,1-c][1,4]benzodiazepine peptoid oligomer libraries. [Portsmouth]: [University of Portsmouth], 2000.

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12

Adams, Lesley Jane. Molecular modelling studies on the pyrrolo[2,1-c][1,4]benzodiazepines. Portsmouth: University of Portsmouth, School of Pharmacy and Biomedical Sciences, 1998.

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13

1957-, Kumar M., and Gupta V. 1966-, eds. Heterocyclic chemistry. Berlin: Springer, 1998.

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14

Heinrich, Karl-Heinz. Untersuchungen zum katalysierten Wasserstoffisotopenaustausch an fünfgliedrigen Heterocyclen vom Furan-, Pyrrol- und Thiophentyp. Leipzig: Akademie der Wissenschaften der DDR, Zentralinstitut für Isotopen- und Strahlenforschung, 1986.

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15

Falk, Heinz. The chemistry of linear oligopyrroles and bile pigments. Wien: Springer-Verlag, 1989.

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16

Gregson, Stephen John. Design, synthesis and evaluation of novel C2-unsaturated pyrrolo[2,1-c][1,4]benzodiazepines. Portsmouth: University of Portsmouth, School of Pharmacy and Biomedical Sciences, 1998.

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17

Roberts, David. The synthesis of pyrrolo[4,3,2-de]quinolines and approaches towards hinckdentine A and apparacine. Manchester: University of Manchester, 1996.

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18

Giochalas, Titos P. Stē gē tou Pyrrou: Diachronikos Hellēnismos stēn Alvania. Athēna: Ekdoseis Asterismos, 1993.

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19

Patel, Sejal. Characterisation of sequence selective binding of the pyrrolo[2,1-c][1,4]benzodiazepine dimers to DNA. Portsmouth: University of Portsmouth, Institute of Biomedical and Biomolecular Sciences, 2000.

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20

Corcoran, Kathryn Elizabeth. Synthetic approaches to C-ring unsaturated DNA cross-linking pyrrolo[2,1-c][1,4]benzodiazepine dimers. Portsmouth: University of Portsmouth, School of Pharmacy and Biomedical Sciences, 1998.

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21

Thompson, Andrew Spencer. Design, synthesis and evaluation of covalent-binding DNA-interactive ligands based on pyrrolo[2,1-c][1,4]benzodiazepines. Portsmouth: University of Portsmouth, School of Pharmacy and Biomedical Sciences, 1992.

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22

Jones, Gary B. Design, synthesis and evaluation of DNA-binding oxazolo[2,3-c][1,4] benzodiazepines and pyrrolo[2,1-c][1,4] benzodiazepines. Portsmouth: Portsmouth Polytechnic, School of Pharmacy and Biomedical Sciences, 1991.

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23

González, Laura Maritza Calderón. Design, synthesis and evaluation of a scaffold and capping units based on the pyrrolo[2,1c][1,4]benzodiazepines for combinatorial chemistry. Portsmouth: University of Portsmouth, School of Pharmacy and Biomedical Sciences, 2000.

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24

Wilson, Stuart Craig. Design, synthesis and biological evaluation of a DNA cross-linking antitumour agent based onthe pyrrolo[2,1-c][1,4]benzodiazepine ring system. Portsmouth: University of Portsmouth, Division of Medicinal Chemistry and Natural Products, 1996.

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25

Puvvada, Madhu. Investigation into the relationship between DNA-binding affinity, sequence-specificity and biological activity in the pyrrolo[2,1-c][1,4]benzodiazepine group of antitumour antibiotics. Portsmouth: University of Portsmouth, Division of Medicinal Chemistry, 1995.

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26

Mason, Elena C., and Allison P. Weber. Polypyrrole: Properties, performance, and applications. Hauppauge, N.Y: Nova Science Publishers, 2010.

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27

Kopecký, Dušan. Deposition of polypyrrole thin films by advanced method: Matrix assisted pulsed laser evaporation. Hauppauge, N.Y: Nova Science Publishers, 2011.

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28

Morris, Stephen James. Design, synthesis and evaluation of a sequence-selective DNA-cleaving agent based on the pyrrolo[2,1-c][1,4]benzodiazepine ring system: Investigation of the DNA-reactive species. Portsmouth: University of Portsmouth, Division of Medicinal Chemistry and Pharmacognosy, 1992.

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29

Derek, Chadwick, Ackrill Kate, and Ciba Foundation, eds. The biosynthesis of the tetrapyrrole pigments. Chichester: Wiley, 1994.

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30

Welch, Colin. Pyrrole: Synthesis and Applications. Nova Science Publishers, Incorporated, 2020.

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31

Gossauer, A. Die Chemie der Pyrrole. Springer, 2012.

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32

Welch, Colin. Pyrrole: Synthesis and Applications. Nova Science Publishers, Incorporated, 2020.

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33

Laurenzo, Kathleen S. Some applications of the synthetic potential of diversely substituted azoles. 1987.

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34

Pyo, Myoungho. Ion transport behavior of polypyrrole during redox switching. 1994.

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35

Florkin, Marcel, and Elmer H. Stotz. Pyrrole Pigments, Isoprenoid Compounds and Phenolic Plant Constituents. Elsevier, 2014.

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36

Jones, Richard A. The Synthesis and the Physical and Chemical Aspects of the Pyrrole Ring, Volume 48, Part 1, Pyrroles. Wiley-Interscience, 1990.

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37

Kawamoto, Yusuke. Synthesis and Biological Evaluation of Pyrrole–Imidazole Polyamide Probes for Visualization of Telomeres. Springer, 2019.

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38

Braun, Robert Collier. Effect of 2(3)-tert-butyl-4-hydroxyanisole and 2-chloroethanol against pyrrole production and chronic toxicity of monocrotaline in chickens. 1985.

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39

Pyrroles. New York: Wiley, 1992.

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40

1935-, Jones R. Alan, ed. Pyrroles. Wiley, 1990.

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41

Eland, John H. D., and Raimund Feifel. Conjugated and aromatic molecules. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198788980.003.0006.

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In the vast majority of conjugated and aromatic molecules, the outermost occupied orbitals are either of π‎ character or non-bonding lone pairs belonging to heteroatoms. These are the orbitals from which double ionisation gives rise to most of the distinct bands that can be discerned in their spectra. Double photoionisation spectra of ethylene, butadiene, pyrrole, furan, thiophene, benzene, hexafluorobenzene, toluene, pyridine, pyrazine, pyrimidine, pyridazine, naphthalene, azulene, quinoline, biphenyl, TDME, iron pentacarbonyl, ferrocene, and TMPPD are presented with analysis where possible. The effects of inner valence Auger effects are also emphasised, which can greatly increase the intensity of double photoionisation. In this chapter, the molecules are ordered mainly in the usual way by number of atoms, then by molecular weight, but the authors have put closely related molecules together where possible.
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42

Chemistry of Pyrroles. Taylor & Francis Group, 2014.

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43

Jones, Richard A. Pyrroles, Part 1. Wiley & Sons, Incorporated, John, 2007.

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44

Trofimov, B. A., Elena Yu Schmidt, Lyubov N. Sobenina, and A. I. Mikhaleva. Chemistry of Pyrroles. Taylor & Francis Group, 2016.

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45

Trofimov, Boris A., Al'bina I. Mikhaleva, Elena Yu Schmidt, and Lyubov N. Sobenina. Chemistry of Pyrroles. Taylor & Francis Group, 2014.

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46

Jones, Richard A. Pyrroles, Part 2. Wiley & Sons, Incorporated, John, 2007.

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47

Trofimov, Boris A., Al'bina I. Mikhaleva, Elena Yu Schmidt, and Lyubov N. Sobenina. Chemistry of Pyrroles. Taylor & Francis Group, 2014.

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48

Jones, Richard A. Pyrroles, Part 1 Vol. 48. Wiley & Sons, Incorporated, John, 2009.

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49

Jones, Richard A. Pyrroles, Part 2 Vol. 48. Wiley & Sons, Incorporated, John, 2009.

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50

Jones, Richard A. The Synthesis, Reactivity, and Physical Properties of Substituted Pyrroles, Volume 48, Part 2, Pyrroles. Wiley-Interscience, 1992.

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