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1. Die Chemie des Pyrrols
by Fischer, Hans and Orth, Hans
1934, 3 v.
Pyrrole
Book
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2. Die Chemie des Pyrrols
by Fischer, Hans and Orth, Hans
1934, 2 v. in 4.
Pyrroles
Book
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3. Full Text Synthesis of Pyrroles by Click Reaction: Silver‐Catalyzed Cycloaddition of Terminal Alkynes with Isocyanides
by Gao, Meng and He, Chuan and Chen, Hongyi and Bai, Ruopeng and Cheng, Ben and Lei, Aiwen
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2013, Volume 52, Issue 27, pp. 6958 - 6961
Just click with silver: Pyrroles are prepared by the co‐cyclization of terminal alkynes and isocyanides in a silver‐catalyzed click reaction. This route... 
click chemistry | silver | terminal alkynes | cycloaddition | pyrroles | ACETYLENES | OLIGOSUBSTITUTED PYRROLES | 1,3-DICARBONYL COMPOUNDS | SUBSTITUTED PYRROLES | EFFICIENT SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY | POLYSUBSTITUTED PYRROLES | AMINES | REGIOSELECTIVE SYNTHESIS | DNA GYRASE | CHEMISTRY | Pyrroles - chemical synthesis | Click Chemistry | Cyanides - chemistry | Pyrroles - chemistry | Carbonates - chemistry | Alkynes - chemistry | Catalysis | Cycloaddition Reaction | Silver Compounds - chemistry | Silver | Cycloaddition | Synthesis | Pyrroles | Formations | Selectivity | Terminals | Alkynes
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4. Full Text Iron(III)-Catalyzed Four-Component Coupling Reaction of 1,3-Dicarbonyl Compounds, Amines, Aldehydes, and Nitroalkanes: A Simple and Direct Synthesis of Functionalized Pyrroles
by Maiti, Sukhendu and Biswas, Srijit and Jana, Umasish
The Journal of Organic Chemistry, ISSN 0022-3263, 03/2010, Volume 75, Issue 5, pp. 1674 - 1683
A simple, convenient, and multicomponent coupling strategy for the synthesis of highly functionalized pyrroles catalyzed by iron(III) salts has been developed.... 
ORGANIC-SYNTHESIS | NATURAL-PRODUCT SYNTHESIS | ONE-POT SYNTHESIS | HIGHLY SUBSTITUTED PYRROLES | PAAL-KNORR REACTION | EFFICIENT SYNTHESIS | CATALYZED REACTION | CHEMISTRY, ORGANIC | MULTICOMPONENT SYNTHESIS | POLYSUBSTITUTED PYRROLES | TETRASUBSTITUTED PYRROLES | Amines - chemistry | Cross-Linking Reagents - chemistry | Pyrroles - chemical synthesis | Magnetic Resonance Spectroscopy | Iron - chemistry | Nitro Compounds | Pyrroles - chemistry | Crystallography, X-Ray | Molecular Structure | Catalysis | Alkanes - chemistry | Aldehydes - chemistry | Analysis | Pyrrole | Substitution reactions | Iron | Chemical properties | Structure
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5. Full Text Silver‐Catalyzed Isocyanide‐Alkyne Cycloaddition: A General and Practical Method to Oligosubstituted Pyrroles
by Liu, Jianquan and Fang, Zhongxue and Zhang, Qian and Liu, Qun and Bi, Xihe
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2013, Volume 52, Issue 27, pp. 6953 - 6957
Ag2CO3 is the key: The transition‐metal‐catalyzed cycloaddition of isocyanides and unactivated terminal alkynes has been realized with Ag2CO3 as a unique and... 
isocyanides | cycloaddition | silver carbonate | oligosubstituted pyrroles | alkynes | ACETYLENES | FURANS | IMINES | COMPLEXES | EFFICIENT SYNTHESIS | TERMINAL ALKYNES | ANTIINFLAMMATORY 4,5-DIARYLPYRROLES | CHEMISTRY, MULTIDISCIPLINARY | ISOCYANOACETATE | DERIVATIVES | C-H | Silver | Pyrroles - chemical synthesis | Cyanides - chemistry | Pyrroles - chemistry | Carbonates - chemistry | Alkynes - chemistry | Catalysis | Cycloaddition Reaction | Silver Compounds - chemistry | Methods | Carbonates | Cycloaddition | Terminals | Catalysts | Pyrroles | Alkynes
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6. Full Text Label-free impedimetric biosensor for Salmonella Typhimurium detection based on poly [pyrrole-co-3-carboxyl-pyrrole] copolymer supported aptamer
by Sheikhzadeh, E and Chamsaz, M and Turner, A.P.F and Jager, E.W.H and Beni, V and Institutionen för fysik, kemi och biologi and Linköpings universitet and Tekniska fakulteten and Biosensorer och bioelektronik
Biosensors and Bioelectronics, ISSN 0956-5663, 06/2016, Volume 80, pp. 194 - 200
The Gram-negative bacterium, is a food borne pathogen responsible for numerous hospitalisations and deaths all over the world. Conventional detection methods... 
Aptamer | Label-free detection | Poly [pyrrole-co-3-carboxyl-pyrrole] | S. Typhimurium | Electrochemical impedance spectroscopy | ELECTROCHEMISTRY | CHEMISTRY, ANALYTICAL | POLYPYRROLE | SENSITIVITY | SENSOR | NANOSCIENCE & NANOTECHNOLOGY | CONDUCTING POLYMERS | BIOPHYSICS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | DNA HYBRIDIZATION | Limit of Detection | Salmonella typhimurium - isolation & purification | Salmonella typhimurium - pathogenicity | Biosensing Techniques | Aptamers, Nucleotide - chemistry | Pyrroles - chemistry | Polymers - chemistry | Food Microbiology | Thiophene | Salmonella typhimurium | Analysis | Salmonella food poisoning | Detectors | Electric properties | Pathogens | Salmonella | Biotechnology | Copolymers | Electrical properties | Foods | Conjugation | Biosensors | Biological Sciences | S. Typhimurium; Aptamer; Electrochemical impedance spectroscopy; Poly [pyrrole-co-3-carboxyl-pyrrole]; Label-free detection | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
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7. Full Text Recent advances in the synthesis of pyrroles by multicomponent reactions
by Estévez, Verónica and Villacampa, Mercedes and Menéndez, J Carlos
Chemical Society reviews, ISSN 0306-0012, 07/2014, Volume 43, Issue 13, pp. 4633 - 4657
Pyrrole is one of the most important one-ring heterocycles. The ready availability of suitably substituted and functionalized pyrrole derivatives is essential... 
Heterocyclic Compounds - chemical synthesis | Pyrroles - chemical synthesis
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8. Full Text Recent advances in the synthesis of pyrroles by multicomponent reactions
by Estévez, Verónica and Villacampa, Mercedes and Menéndez, J. Carlos
Chemical Society Reviews, ISSN 0306-0012, 6/2014, Volume 43, Issue 13, pp. 4633 - 4657
Pyrrole is one of the most important one-ring heterocycles. The ready availability of suitably substituted and functionalized pyrrole derivatives is essential... 
CONVENIENT SYNTHESIS | ONE-POT SYNTHESIS | HIGHLY SUBSTITUTED PYRROLES | 1,3-DICARBONYL COMPOUNDS | PROPARGYLIC ALCOHOLS | PROMOTED 3-COMPONENT REACTION | PRIMARY AMINES | FUNCTIONALIZED PYRROLES | EFFICIENT | CHEMISTRY, MULTIDISCIPLINARY | POLYSUBSTITUTED PYRROLES | Availability | Synthesis (chemistry) | Pyrroles | Materials science | Biology | Derivatives | Access routes
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9. Full Text Pyrrole: An emerging scaffold for construction of valuable therapeutic agents
by Gholap, Somnath S
European Journal of Medicinal Chemistry, ISSN 0223-5234, 03/2016, Volume 110, pp. 13 - 31
Pyrrole derivatives comprise a class of biologically active heterocyclic compounds which can serve as promising scaffolds for antimicrobial, antiviral,... 
Therapeutic agents | N-substituted pyrrole | Fused pyrroles | Natural pyrrole derivatives | DESIGN | CHEMISTRY, MEDICINAL | DISCOVERY | IN-VITRO | POTENT | ANTICANCER | BIOLOGICAL EVALUATION | NITRIC-OXIDE | DERIVATIVES | ANTIMICROBIAL ACTIVITY | INHIBITING ACTIVITY | Pyrroles - pharmacokinetics | Antioxidants - chemistry | Anti-Infective Agents - pharmacology | Humans | Enzyme Inhibitors - pharmacology | Structure-Activity Relationship | Antioxidants - pharmacology | Antineoplastic Agents - chemistry | Drug Discovery | Animals | Anti-Infective Agents - chemistry | Enzyme Inhibitors - chemistry | Pyrroles - chemistry | Antineoplastic Agents - pharmacology | Antiviral agents | Enzymes | Thiophene | Heterocyclic compounds | Health aspects | Antioxidants | Enzyme inhibitors
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10. Full Text Regulation of kynurenine biosynthesis during influenza virus infection
by Gaelings, Lana and Söderholm, Sandra and Bugai, Andrii and Fu, Yu and Nandania, Jatin and Schepens, Bert and Lorey, Martina B and Tynell, Janne and Vande Ginste, Liesbeth and Le Goffic, Ronan and Miller, Matthew S and Kuisma, Marika and Marjomäki, Varpu and De Brabander, Jef and Matikainen, Sampsa and Nyman, Tuula A and Bamford, Dennis H and Saelens, Xavier and Julkunen, Ilkka and Paavilainen, Henrik and Hukkanen, Veijo and Velagapudi, Vidya and Kainov, Denis E
The FEBS Journal, ISSN 1742-464X, 01/2017, Volume 284, Issue 2, pp. 222 - 236
Influenza A viruses (IAVs) remain serious threats to public health because of the shortage of effective means of control. Developing more effective virus... 
influenza virus | innate immunity | interferon | indoleamine‐pyrrole 2,3‐dioxygenase (IDO1) | host–pathogen interaction | indoleamine-pyrrole 2,3-dioxygenase (IDO1) | host-pathogen interaction | CELLS | HUMAN MACROPHAGES | BIOCHEMISTRY & MOLECULAR BIOLOGY | INDOLEAMINE 2,3-DIOXYGENASE | A VIRUS | RESPONSES | NS1 PROTEIN | INHIBITION | REPLICATION | SALIPHENYLHALAMIDE | EXPRESSION | Indoleamine-Pyrrole 2,3,-Dioxygenase - genetics | Humans | Kynurenine - biosynthesis | Transcriptome | Indoleamine-Pyrrole 2,3,-Dioxygenase - immunology | Interferons - immunology | Influenza A Virus, H1N1 Subtype - growth & development | Tryptophan - metabolism | Lung - virology | Macrophages - virology | Metabolic Networks and Pathways - immunology | Female | Interferons - genetics | Influenza A Virus, H1N1 Subtype - genetics | Influenza A Virus, H1N1 Subtype - metabolism | Orthomyxoviridae Infections - drug therapy | Antiviral Agents - pharmacology | Orthomyxoviridae Infections - pathology | Gene Expression Regulation | Viral Nonstructural Proteins - genetics | Influenza A Virus, H1N1 Subtype - drug effects | Sulfonamides - pharmacology | Host-Pathogen Interactions | Metabolic Networks and Pathways - genetics | Pyrroles - pharmacology | Animals | Virus Replication | Kynurenine - antagonists & inhibitors | Lung - drug effects | Oximes - pharmacology | Macrophages - drug effects | Viral Nonstructural Proteins - metabolism | Mice | Mice, Inbred BALB C | Oxazoles - pharmacology | Thiazoles - pharmacology | Metabolic Networks and Pathways - drug effects | Primary Cell Culture | Orthomyxoviridae Infections - virology | Immunologic Factors - pharmacology | Indoleamine-Pyrrole 2,3,-Dioxygenase - antagonists & inhibitors | Lung - immunology | Orthomyxoviridae Infections - immunology | Influenza viruses | Influenza | Physiological aspects | Interferon | Biological response modifiers | T cells | Health aspects | Antibacterial agents | Viruses | Infections | Biosynthesis | Drugs | Lymphocytes T | Drug development | Macrophages | Antiinfectives and antibacterials | Lipopolysaccharides | Control | Pain | Bacteria | Attenuation | Inhibition | Public health | Antiviral agents | Dioxygenase | Pathogens | Hypersensitivity | Host-pathogen interactions | Replication | NS1 protein | Stimuli
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11. From a seaside town
by Levine, N
1970, 220
Book
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12. Hetero-aromatic nitrogen compounds
: pyrroles and pyridines
by Schofield, Kenneth
1967, viii, 434
Pyridine | Pyrroles
Book
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13. Full Text Catalytic C−H Arylation of SEM-Protected Azoles with Palladium Complexes of NHCs and Phosphines
by Touré, B. Barry and Lane, Benjamin S and Sames, Dalibor
Organic Letters, ISSN 1523-7060, 05/2006, Volume 8, Issue 10, pp. 1979 - 1982
The synthesis and catalytic evaluation of palladium complexes containing imidazolyl carbene ligand of varying steric and electronic properties is reported.... 
PYRROLE | CHEMISTRY, ORGANIC | INDOLES
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14. Full Text Design, synthesis and biological evaluation of 3-substituted 2,5-dimethyl-N-(3-(1H-tetrazol-5-yl)phenyl)pyrroles as novel potential HIV-1 gp41 inhibitors
by He, Xiao-Yang and Zou, Peng and Qiu, Jiayin and Hou, Ling and Jiang, Shibo and Liu, Shuwen and Xie, Lan
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 11/2011, Volume 19, Issue 22, pp. 6726 - 6734
Based on the structure of HIV-1 gp41 binding site for small-molecule inhibitors, optimization of lead resulted in the discovery of a new series of 2,5... 
3-Substituted 2,5-dimethyl-N-(3-tetrazol-5-yl)phenyl)pyrrole derivatives | Small-molecule fusion inhibitors | HIV-1 gp41 | Anti-HIV agents | 3-Substituted 2,5-dimethyl-N-(3-tetrazol- 5-yl)phenyl)pyrrole derivatives | CHEMISTRY, MEDICINAL | ENTRY INHIBITORS | FUSION | 3-Substituted 2,5-dimethyl-N-(3-tetrazol-5yl)phenyl)pyrrole derivatives | CAVITY | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, ORGANIC | TARGETING GP41 | SUBSTITUTED PYRROLE DERIVATIVES | IMMUNODEFICIENCY-VIRUS TYPE-1 | CORE STRUCTURE | COILED-COIL | Anti-HIV Agents - pharmacology | HIV-1 - metabolism | Tetrazoles - chemical synthesis | Tetrazoles - pharmacology | Humans | Structure-Activity Relationship | HIV Envelope Protein gp41 - antagonists & inhibitors | HIV Envelope Protein gp41 - chemistry | Anti-HIV Agents - chemistry | Pyrroles - pharmacology | Pyrroles - chemical synthesis | Pyrroles - chemistry | Binding Sites | Index Medicus
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15. Full Text Preparation of Tetrasubstituted 3‑Phosphonopyrroles through Hydroamination: Scope and Limitations
by Debrouwer, Wouter and Heugebaert, Thomas S. A and Stevens, Christian V
The Journal of Organic Chemistry, ISSN 0022-3263, 05/2014, Volume 79, Issue 10, pp. 4322 - 4331
Phosphonylated pyrroles were obtained by a ZnCl2-catalyzed 5-exo-dig hydroamination of propargylic enamines. These starting compounds were obtained in two... 
AMINATION/ANNULATION REACTIONS | OLIGOSUBSTITUTED PYRROLES | HIGHLY SUBSTITUTED PYRROLES | INTERMOLECULAR HYDROAMINATION | INTRAMOLECULAR HYDROAMINATION | 2-PROPYNYL-1,3-DICARBONYL COMPOUNDS | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | FUNCTIONALIZED PYRROLES | POLYSUBSTITUTED PYRROLES | CATALYZED HYDROAMINATION | Organophosphorus Compounds - chemical synthesis | Pyrroles - chemical synthesis | Amination | Cyclization | Halogenation | Pyrroles - chemistry | Organophosphorus Compounds - chemistry | Molecular Structure | Catalysis | Chemical properties | Research | Pyrrole | Amino compounds
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16. Full Text Direct Synthesis of Pyrroles by Dehydrogenative Coupling of -Aminoalcohols with Secondary Alcohols Catalyzed by Ruthenium Pincer Complexes
by Srimani, D and Ben-David, Y and Milstein, D
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, ISSN 1433-7851, 2013, Volume 52, Issue 14, pp. 4012 - 4015
Pyrroles were synthesized in one step by using the acceptorless dehydrogenative coupling of amino alcohols with secondary alcohols (equivalent amounts),... 
3-COMPONENT SYNTHESIS | ONE-POT SYNTHESIS | HIGHLY SUBSTITUTED PYRROLES | PAAL-KNORR REACTION | pincer complex | EFFICIENT SYNTHESIS | METAL-LIGAND COOPERATION | pyrroles | CHEMISTRY, MULTIDISCIPLINARY | ruthenium | SEQUENTIAL REACTIONS | homogeneous catalysis | DUOCARMYCIN DERIVATIVES | dehydrogenation | FUNCTIONALIZED PYRROLES | TETRASUBSTITUTED PYRROLES | Dehydrogenation | Ruthenium | Synthesis | Equivalence | Pyrroles | Joining | Bonding | Alcohols
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17. Biosynthesis of tetrapyrroles
by Jordan, P. M
1991, New comprehensive biochemistry, ISBN 0444892850, Volume 19., xii, 309
Synthèse | Synthesis | Tétrapyrroles | Tetrapyrroles
Book
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18. Full Text Improved BM212 MmpL3 Inhibitor Analogue Shows Efficacy in Acute Murine Model of Tuberculosis Infection
by Poce, Giovanna and Bates, Robert H and Alfonso, Salvatore and Cocozza, Martina and Porretta, Giulio Cesare and Ballell, Lluís and Rullas, Joaquin and Ortega, Fátima and De Logu, Alessandro and Agus, Emanuela and La Rosa, Valentina and Pasca, Maria Rosalia and De Rossi, Edda and Wae, Baojie and Franzblau, Scott G and Manetti, Fabrizio and Botta, Maurizio and Biava, Mariangela
PLoS ONE, ISSN 1932-6203, 02/2013, Volume 8, Issue 2, p. e56980
1,5-Diphenyl pyrr