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Relevant bibliographies by topics / Benzo[b]-1

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Academic literature on the topic 'Benzo[b]-1'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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Journal articles on the topic "Benzo[b]-1"

1

Arul Clement, J., Pethaiah Gunasekaran, and Arasambattu K. Mohanakrishnan. "Synthesis and characterization of benzo[c]thiophene analogs incorporating benzo[b]thiophene/1-hexylindole/benzo[b]furan." Tetrahedron 65, no. 21 (2009): 4113–23. http://dx.doi.org/10.1016/j.tet.2009.03.059.

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BHASKAR, J. UDAYA, G. SRINIVASA RAO, B. PULLA RAO, PRANAB CHATTERJEE, D. K. SAHOO, and S. SRINIVASA RAO. "Design, Synthesis, Structural Characterization and Antimicrobial Screening of Several Novel Benzothiophene Linked Thiazolidines." Asian Journal of Chemistry 35, no. 9 (2023): 2176–80. http://dx.doi.org/10.14233/ajchem.2023.27958.

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A novel sequence of (19E)-(3-(benzo[b]thiophen-3-yl)-N′-((Z)-5-benzyliden-4-oxo-3-phenyl thiazolidin-2-ylidene)propanehydrazides (6a-f) was synthesized in moderate to good yields from the final intermediate, (E)-(3-(benzo[b]thiophen-3-yl)-N′-(4-oxo-3-phenylthiazolidin- 2-ylidene)propane hydrazide (5). In present work, 3-(benzo[b]thiophen-3-yl)propanoic acid (1) was selected as raw material and compounds such as 1-(benzo[b]thiophen-3-yl)pentan-3-one (2), 3-(benzo[b]thiophen-3-yl)propanehydrazide (3) and 1-(3-(benzo[b]- thiophen-3-yl)-propanoyl)-4-phenylsemicarbazide (4) were materialized as int

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Truong, Minh Anh, and Koji Nakano. "Syntheses of dibenzo[d,d']benzo[2,1-b:3,4-b']difuran derivatives and their application to organic field-effect transistors." Beilstein Journal of Organic Chemistry 12 (April 26, 2016): 805–12. http://dx.doi.org/10.3762/bjoc.12.79.

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Ladder-type π-conjugated compounds containing a benzo[2,1-b:3,4-b']difuran skeleton, such as dibenzo[d,d']benzo[2,1-b:3,4-b']difuran (syn-DBBDF) and dinaphtho[2,3-d:2',3'-d']benzo[2,1-b:3,4-b']difuran (syn-DNBDF) were synthesized. Their photophysical and electrochemical properties were revealed by UV–vis absorption and photoluminescence spectroscopy and cyclic voltammetry. Organic field-effect transistors (OFETs) were fabricated with these compounds as organic semiconductors, and their semiconducting properties were evaluated. OFETs with syn-DBBDF and syn-DNBDF showed typical p-type characteri

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4

Portilla, Jaime, Jairo Quiroga, Manuel Nogueras, et al. "Structural comparisons of isomeric series of 7-aryl-benzo[h]pyrazolo[3,4-b]quinolines and 11-aryl-benzo[f]pyrazolo[3,4-b]quinolines." Acta Crystallographica Section B Structural Science 64, no. 1 (2008): 72–83. http://dx.doi.org/10.1107/s0108768107065743.

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The structures of three new 7-aryl-benzo[h]pyrazolo[3,4-b]quinolines, 8-methyl-7-(4-chlorophenyl)-10-phenyl-6,10-dihydro-5H-benzo[h]pyrazolo[3,4-b]quinoline, C27H20ClN3, 8-methyl-7-(3-pyridinyl)-10-phenyl-6,10-dihydro-5H-benzo[b]pyrazolo[3,4-b]quinoline, C26H20N4, and 8-methyl-7-(4-pyridinyl)-10-phenyl-10H-benzo[h]pyrazolo[3,4-b]quinoline, C26H18N4, which is an unexpected oxidation product isolated from the attempted synthesis of 8-methyl-7-(4-pyridinyl)-10-phenyl-6,10-dihydro-5H-benzo[h]pyrazolo[3,4-b]quinoline, and those of three new 11-aryl-benzo[f]pyrazolo[3,4-b]quinolines, 11-(4-methylphe

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Acosta Quintero, Lina M., Isidro Burgos, Alirio Palma, Justo Cobo, and Christopher Glidewell. "A concise, efficient and versatile synthesis of amino-substituted benzo[b]pyrimido[5,4-f]azepines: synthesis and spectroscopic characterization, together with the molecular and supramolecular structures of three products and one intermediate." Acta Crystallographica Section C Structural Chemistry 74, no. 3 (2018): 312–20. http://dx.doi.org/10.1107/s2053229618002176.

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A concise, efficient and versatile synthesis of amino-substituted benzo[b]pyrimido[5,4-f]azepines is described: starting from a 5-allyl-4,6-dichloropyrimidine, the synthesis involves base-catalysed aminolysis followed by intramolecular Friedel–Crafts cyclization. Four new amino-substituted benzo[b]pyrimido[5,4-f]azepines are reported, and all the products and reaction intermediates have been fully characterized by IR,1H and13C NMR spectroscopy and mass spectrometry, and the molecular and supramolecular structures of three products and one intermediate have been determined. In each ofN,2,6,11-t

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Wojciechowski, Krzysztof, and Michał Nowacki. "Synthesis of [1]Benzothieno[2,3-b]quinolines via Transition-Metal-Free [3+3] Annulation of Nitroarenes and Benzo[b]thiophen-3-ylacetonitrile or 3-(Phenylsulfonylmethyl)benzo[b]thiophene Carbanions." Synthesis 49, no. 16 (2017): 3794–800. http://dx.doi.org/10.1055/s-0036-1588426.

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Benzo[b]thiophen-3-ylacetonitriles or 3-(phenylsulfonylmethyl)benzo[b]thiophenes react with nitrobenzene derivatives in the presence of potassium tert-butoxide and chlorotrimethylsilane to form, in good yields, 11-cyano- or 11-(phenylsulfonyl)[1]benzothieno[2,3-b]quinolines, respectively.

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El-Agrody, Ahmed M., Fathy A. Eid, Hussein A. Emam, Hany M. Mohamed, and Ahmed H. Bedair. "Synthesis of 9-Methoxy and 9-Acetoxy-3-amino-1-(4-methoxyphenyl)- 1H-benzo[f]chromene-2-carbonitriles via 2-(Imino-piperidin-1-yl-methyl)- 3-(4-methoxyphenyl)acrylonitrile as Intermediate." Zeitschrift für Naturforschung B 57, no. 5 (2002): 579–85. http://dx.doi.org/10.1515/znb-2002-0516.

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Several new 1H-benzo[f]chromene derivatives (3aÐd) were prepared by the reaction of 7-substituted-2-naphthols (1a,b) with substituted α-cyano-4-methoxycinnamonitriles (2a,b) together with 2-(imino-piperidin-1-yl-methyl)-3-(4-methoxyphenyl)acrylonitrile (4) as intermediate. Also, the reaction of 1a,b with 4 without catalyst afforded 9-methoxy and 9-acetoxy- 3-amino-1-(p-methoxyphenyl)-1H-benzo[f]chromene-2-carbonitrile (3b,e). The reaction of 3a,b with different electrophilic and nucleophilic reagents afforded the 12H-7-oxa-8,10-diazabenzo[ a]anthracene derivatives 5, 9, 10 and 1H-benzo[f]chrom

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Kachhadia, V. V., M. R. Patel, and H. S. Joshi. "Heterocyclic systems containing S/N regioselective nucleophilic competition: Facile synthesis, antitubercular and antimicrobial activity of thiohydantoins and iminothiazolidinones containing the benzo." Journal of the Serbian Chemical Society 70, no. 2 (2005): 153–61. http://dx.doi.org/10.2298/jsc0502153k.

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The required compounds N-aryl-N'-(3-chloro-2-benzo[b]thenoyl)-thioureas 1a-k were prepared by condensing 3-chloro-2-benzo[b]thenoyl chloride with different arylamines using ammonium thiocyanate, which in turn when treated with chloroacetic acid, yielded 1-aryl-3-(3-chloro-2-benzo[b]thenoyl)thiohydantoins 2a-k, while in the presence of sodium acetate treated with chloroacetic acid, yielded 2-arylimino-3-(3-chloro-2-benzo[b]thenoyl)-4-thiazolidinones 3a-k. All the synthesized compounds were screened for their antitubercular and antimicrobial activities. Some selected compounds were selected for

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Ryu, Seunghyup, Chaeyoung Yun, Soomin Ryu, Jihae Ahn, Choongik Kim, and Sungyong Seo. "Characterization of [1]Benzothieno[3,2-b]benzothiophene (BTBT) Derivatives with End-Capping Groups as Solution-Processable Organic Semiconductors for Organic Field-Effect Transistors." Coatings 13, no. 1 (2023): 181. http://dx.doi.org/10.3390/coatings13010181.

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Solution-processable [1]benzothieno[3,2-b]benzothiophene (BTBT) derivatives with various end-capping groups, 2-(phenylethynyl)benzo[b]benzo[4,5]thieno[2,3-d]thiophene (Compound 1), 2-octyl-7-(5-(phenylethynyl)thiophen-2-yl)benzo[b]benzo[4,5]thieno[2,3-d]thiophene (Compound 2), and triisopropyl((5-(7-octylbenzo[b]benzo[4,5]thieno[2,3-d]thiophen-2-yl)thiophen-2-yl)ethynyl)silane (Compound 3), have been synthesized and characterized as active layers for organic field-effect transistors (OFETs). Thermal, optical, and electrochemical properties of the newly synthesized compounds were characterized

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Katzsch, Felix, Tobias Gruber, and Edwin Weber. "Crystal structures of functional building blocks derived from bis(benzo[b]thiophen-2-yl)methane." Acta Crystallographica Section C Structural Chemistry 72, no. 9 (2016): 679–84. http://dx.doi.org/10.1107/s2053229616012973.

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The syntheses of three bis(benzo[b]thiophen-2-yl)methane derivatives, namely bis(benzo[b]thiophen-2-yl)methanone, C17H10OS2, (I), 1,1-bis(benzo[b]thiophen-2-yl)-3-(trimethylsilyl)prop-2-yn-1-ol, C22H20OS2Si, (II), and 1,1-bis(benzo[b]thiophen-2-yl)prop-2-yn-1-ol, C19H12OS2, (III), are described and their crystal structures discussed comparatively. The conformation of ketone (I) and the respective analogues are rather similar for most of the compounds compared. This is true for the interplanar angles, the Caryl—Cbridge—Carylangles and the dihedral angles. The best resemblance is found for a bio

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Dissertations / Theses on the topic "Benzo[b]-1"

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Moulin, Claudie. "Trois,quatre-dihydro-2h-1-benzo(b)pyrane-2-carboxamides analogues du trolox et derives a potentialites anti-allergique ou antidiabetique." Nantes, 1996. http://www.theses.fr/1996NANT12VS.

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Bezerra, Fernando Antonio Frota. "Estudo fase I do cloridrato do (1R, 2R)-(+)-N-metil-N-[2 (1-pirrolidinil) ciclohexil] benzo [B] tiofeno-4-acetamida (RSD921) em voluntarios sadios do sexo masculino." [s.n.], 1999. http://repositorio.unicamp.br/jspui/handle/REPOSIP/309478.

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Orientador: Gilberto de Nucci<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas<br>Made available in DSpace on 2018-07-25T01:34:25Z (GMT). No. of bitstreams: 1 Bezerra_FernandoAntonioFrota_M.pdf: 5664148 bytes, checksum: 90d4a93cd491100a95bae357558dfca4 (MD5) Previous issue date: 1999<br>Resumo: O presente trabalho,um ensaio clínico Fase I, aberto, com doses únicas crescentes. teve como propósitos avaliar, em voluntários humanos sadios, a tolerância, a segurança, possíveis efeitos farmacodinâmicos e o perfil farmacocinético do Cloridrato de (1R,2R)

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González, Lira Christian Guillermo. "Estudio de Funcionalización de la (4-Nitro-Fenil)-1-Piperazina Orientada a la Síntesis de (4,7-Dimetoxi-Benzo[b]Tiofen-2-Carbonil) Piperazinil Arilbenzamidas como Potenciales Ligandos Serotoninérgicos." Tesis, Universidad de Chile, 2007. http://www.repositorio.uchile.cl/handle/2250/105666.

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Memoria para optar al título de Químico<br>Las arilpiperazinas constituyen una familia de compuestos de interés en el ámbito neurofarmacológico principalmente por sus acciones ansiolíticas y antidepresivas, a través de interacciones con el receptor serotoninérgico 5-HT1A. El presente trabajo de tesis informa de la síntesis de una serie de compuestos benzotiofenarilpiperazínicos 10 (a-f) adecuadamente funcionalizados. El acceso sintético a esta serie tiene lugar a través de una secuencia de 6 pasos a partir de 3,6-dimetoxi-2-nitrobenzaldehído con tioglicolato de metilo en medio básico. Como p

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4

Martin-Fardon, Rémi. "Effets comparés de traitements chroniques par la cocai͏̈ne et la N-[1-(2-benzo(B)thiophényl)cyclohexyl]pipéridine (BTCP), sur la concentration extracellulaire de dopamine dans le striatum de rat." Montpellier 2, 1996. http://www.theses.fr/1996MON20186.

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La microdialyse repetee chez un meme animal permet la mesure a long terme de la concentration de dopamine (da) extracellulaire (dae, 10 fois sur une periode de 23 jours) dans le striatum. La cocaine et la btcp sont des inhibiteurs de la recapture de la da. Aux doses respectives de 20 et 10 mg/kg elles ont des effets comportementaux et sur le niveau de base de da dans le striatum et le nucleus accumbens, similaires. La dialyse repetee a ete appliquee a la mesure d'effets de traitements chroniques (tch) par la cocaine (20 mg/kg), la btcp (10 mg/kg) et croises (tcr). Le premier jour du tch, les d

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Zhang, Bei. "STUDY OF THE EFFECT OF STERIC BULK OF SIDE CHAINS ON THE PROPERTIES OF CONJUGATED POLYMERS." UKnowledge, 2018. https://uknowledge.uky.edu/chemistry_etds/95.

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Donor-acceptor conjugated polymers opened a new era for conjugated polymer research due to the abundant selection and combination of diﬀerent conjugated units. This class of polymers function as semiconductor materials with potential application in plastic consumer electronics. The frontier molecular orbital energies of the polymers are generally determined by the selection of donor and acceptor units in the backbone structure, and their substituents. The side chains attached to the backbone not only affect the solubility of the materials, but also their self-assembly and morphological charact

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Seltmann, Jens. "Struktur-Eigenschaftsbeziehungen V-förmiger Mesogene zur Realisierung biaxial nematischer Mesophasen." Doctoral thesis, Universitätsbibliothek Chemnitz, 2011. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-67693.

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Die vorliegende Arbeit befasst sich mit der Synthese und der Untersuchung von Struktur-Eigenschaftsbeziehungen neuartiger V-förmiger, formstabiler Mesogene zur Realisierung biaxial nematischer Mesophasen (Nb). Alle synthetisierten Verbindungen besitzen ein formtreues Oligo(phenylenethinylen)-Grundgerüst, an welches laterale Alkyloxyketten und verschiedene terminale Substituenten (z. B. -CN, O(CH2)nCOOEt, Pyridyle) angebunden wurden. Durch dieses spezielle Design erhält man ausschließlich nematische und keine höher geordneten flüssigkristallinen Phasen. Durch den Einsatz verschiedener zentraler

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Deleuze, Carine. "Le chlorhydrate de 1-[1-(2-benzo[b]thiophényl]pipéridine (BTCP), un puissant inhibiteur de capture neuronale de dopamine, donne deux métabolites primaires actifs in vitro et in vivo : Synthèse, identification et quantification des métabolites obtenus à partir de microsomes de foie, de tissus cérébraux, de plasma et d'urines." Montpellier 1, 1998. http://www.theses.fr/1998MON13508.

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Lin, Hsiao-Yu, and 林小玉. "Pyrolytic Study of 2-Azido-1-(1-methyl-2-pyrryl)ethanone and 2-Azido-1-(2-benzo[b]thienyl)ethanone." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/11889651935762953739.

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碩士<br>國立中山大學<br>化學系研究所<br>91<br>Flash vacuum pyrolysis (FVP) of 2-azido-1-(1-methyl-2-pyrryl)ethanone and 2-azido-1- (2-benzo[b]thienyl)ethanone gave nitrene by elimination of one nitrogen molecule. When 2-azido-1-(1-methyl-2-pyrryl)ethanone as a precorsor, the reactive nitrene readily underwent self-condensation to give 2-(1-methyl-2-formylpyrryl)-4-(1-methyl-2- pyrryl)imidazole, it’s isomer and 2,4,5-tri(1-methyl-2-formylpyrryl) imidazole. While 2-azido-1-(2-benzo[b]thienyl)ethanone as a precorsor, the reactive nitrene readily underwent self-condensation to give 2-2-formylbenzo[b]thienyl-

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Books on the topic "Benzo[b]-1"

1

Gröschl, Dieter. Benzoanellierte-Heterocyclen durch Umsetzung von 2H-1-Benzo[b]thiet. 1995.

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Decker-Burgard, Sabine. Antimutagene Effekte verschiedener Apfeisorten, Orangen- und Grapefruitchargen im Salmonella/Reversions-Test gegenüber den Mutagenen 2-Amino-3-methylimidazo (4, 5-f)chinolin (IQ), 2-Amino-1-methyl-6-phenylimidazo (4, 5-b)pyridin (PhIP), Benzo(a)pyren, 2-Nitrofluoren, 2,4,7-Trinitro-9-fluorenon, Natriumazid, [beta]-Propiolacton und Captafol. 1995.

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Book chapters on the topic "Benzo[b]-1"

1

Joule, J. A., K. Mills, and G. F. Smith. "Benzo[b]thiophenes and benzo[b]furans: reactions and synthesis." In Heterocyclic Chemistry. Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8_18.

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Joule, J. A., K. Mills, and G. F. Smith. "Reactivity of indoles, benzo[b]thiophenes, benzo[b]furans, isoindoles, benzo[c]thiophenes and isobenzofurans." In Heterocyclic Chemistry. Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8_16.

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Li, Huanhuan, Kailin Han, Qiannan Guo, Fengxi Liu, Peng Yu, and Yuou Teng. "Design, Synthesis and Biological Evaluation of the Novel Antitumor Agent 2H-benzo[b][1, 4]oxazin-3(4H)-one and Its Derivatives." In Lecture Notes in Electrical Engineering. Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-7618-0_382.

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Banupriya, K., and B. Preethi. "Synthesis, Anticancer Evaluation, and Molecular Docking Studies of Novel 1-Phenyl-3A,9-Dihydro-1H-Benzo[E]Tetrazolo[5,1-b][1,3]Thiazine with the Inhibitor." In Springer Proceedings in Physics. Springer Nature Switzerland, 2024. https://doi.org/10.1007/978-3-031-69970-2_22.

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Mukhtar, H., M. Das, and D. R. Bickers. "Alterations in Benzo(a)Pyrene Metabolism and its DNA Adduct Formation in Skin of Mice Chronically Exposed to Ultraviolet-B Radiation." In Radiation Carcinogenesis and DNA Alterations. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5269-3_14.

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"Product Class 1: Benzo[b]furans." In Knowledge Updates 2014/4, edited by Banert, Hall, Joule, Moloney, Reissig, and Schaumann. Georg Thieme Verlag, 2015. http://dx.doi.org/10.1055/sos-sd-101-00568.

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"Product Class 1: Benzo[b]furans." In Category 2, Hetarenes and Related Ring Systems, edited by Thomas. Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/sos-sd-010-00002.

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"Product Class 1: Benzo[b]furans." In Knowledge Updates 2014/4, edited by K. Banert, D. G. Hall, J. A. Joule, M. G. Moloney, H. U. Reissig, and E. Schaumann. Georg Thieme Verlag, 2015. http://dx.doi.org/10.1055/sos-sd-110-00529.

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T. Pham, Phuong-Truc, and Mamoun M. Bader. "Design of Novel Functional Materials Using Reactions of Quinones with Aromatic Amines." In Novelties in Schiff Bases [Working Title]. IntechOpen, 2024. http://dx.doi.org/10.5772/intechopen.114301.

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This chapter presents examples for the successful use of Schiff base chemistry in the molecular design and synthesis of novel organic semiconductors composed of fused heterocyclic ladder oligomers as an alternative for oligoacenes. The materials resulting from reacting quinones with aryl amines (Schiff Bases) have proven to possess favorable properties for applications when compared with their oligoacene counterparts, including pentacene. Molecules obtained from reactions of 2,5- dichloro-1,4-benzoquinone and 2,3-dichloro-1,4-naphtoquinone with 2-aminophenols and 2-aminothiophenols discussed i

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Weeks, Stephan, Arthur P. D’Silva, and Roy L. M. Dobson. "Multidimensional, Resonance-Enhanced Multiphoton Ionization Time-of-Flight Mass Spectrometry for Characterizing Environmental and Biological Samples for Polycyclic Aromatic Compounds." In Lasers and Mass Spectrometry. Oxford University PressNew York, NY, 1990. http://dx.doi.org/10.1093/oso/9780195059298.003.0023.

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Abstract Analysis of environmental samples for polycyclic aromatic compounds (PACs) is the proverbial tip of the iceberg. These compounds are ubiquitous. The potential human health hazard of some PACs, such as the infamous benzo[a]pyrene (B[a]P), as mutagens and carcinogens is well established.1 Common wisdom dictates the development of analytical methods that allow studies determining the sources of these potential carcinogenic compounds, their transport in the environment, and, finally, the metabolism to their ultimate carcinogenic form.

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Conference papers on the topic "Benzo[b]-1"

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Nikhila, G. R., S. R. Batakurki, and B. C. Yallur. "Synthesis, characterization and antioxidant studies of benzo[4, 5]imidazo[2, 1-b]thiazole derivatives." In PROCEEDINGS OF INTERNATIONAL CONFERENCE ON ADVANCES IN MATERIALS RESEARCH (ICAMR - 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0023101.

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Sampaio, Geni Rodrigues, Simone Alves da Silva, Adriana Palma de Almeida, Glória Maria Guizellini, Marcelo Macedo Rogero, and Elizabeth Aparecida Ferraz da Silva Torres. "Determinação de HPAs em amostras de salsicha e hambúrguer comercializadas na cidade de São Paulo." In Congresso dos Profissionais das Universidades Estaduais de São Paulo. Universidade Estadual de Campinas. Sistema de Bibliotecas, 2023. http://dx.doi.org/10.20396/conpuesp.2.2023.4973.

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Introdução: Os hidrocarbonetos policíclicos aromáticos representam uma classe de cerca de 200 compostos, e são contaminantes orgânicos formados por anéis aromáticos condensados (Khalili et al., 2023). São conhecidos pelas propriedades mutagênicas e carcinogênicas, sendo o benzo(a)pireno (BaP) conhecido como o principal composto carcinogênico classificado no grupo 1 da Agência Internacional de Pesquisas em Câncer (IARC, 2010, 2012). Os humanos estão expostos aos HPAs através de diversas vias, sendo os alimentos a principal com 88–98% da exposição total (Samiee et al., 2020). A contaminação dos

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Harris, Kenneth J., Kelly L. Harris, Mary K. Washington, James Amos-Landgraf, and Aramandla Ramesh. "Abstract 4804: Sex-specific differences in Benzo(a)Pyrene [B(a)P]-induced colon carcinogenesis." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-4804.

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