Log in

Relevant bibliographies by topics / Fused Benzimidazoles / Journal articles

To see the other types of publications on this topic, follow the link: Fused Benzimidazoles.

Journal articles on the topic 'Fused Benzimidazoles'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Fused Benzimidazoles.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Sweeney, Martin, Darren Conboy, Styliana I. Mirallai, and Fawaz Aldabbagh. "Advances in the Synthesis of Ring-Fused Benzimidazoles and Imidazobenzimidazoles." Molecules 26, no. 9 (2021): 2684. http://dx.doi.org/10.3390/molecules26092684.

Full text

Abstract:

This review article provides a perspective on the synthesis of alicyclic and heterocyclic ring-fused benzimidazoles, imidazo[4,5-f]benzimidazoles, and imidazo[5,4-f]benzimidazoles. These heterocycles have a plethora of biological activities with the iminoquinone and quinone derivatives displaying potent bioreductive antitumor activity. Synthesis is categorized according to the cyclization reaction and mechanisms are detailed. Nitrobenzene reduction, cyclization of aryl amidines, lactams and isothiocyanates are described. Protocols include condensation, cross-dehydrogenative coupling with trans

APA, Harvard, Vancouver, ISO, and other styles

2

Kumar, Sushil, Maneesha D. Sati, and S. C. Sati. "Synthesis And Biological Evaluation Of Benzimidazole Derivatives." IOSR Journal of Applied Chemistry 17, no. 12 (2024): 13–18. https://doi.org/10.9790/5736-1712011318.

Full text

Abstract:

Benzimidazoles are a class of heterocyclic compounds in which a benzene ring is fused to the 4 and 5 positions of an imidazole ring. Benzimidazole refers to the parent compound, while benzimidazoles are a class of heterocyclic compounds having similar ring structures, but different substituents. Benzimidazole derivatives possess a wide range of bioactivities including antimicrobial, anthelmintic, antiviral, anticancer, and antihypertensive activities. Many compounds possessing a benzimidazole skeleton have been employed as drugs in the market. The application of benzimidazoles in other fields

APA, Harvard, Vancouver, ISO, and other styles

3

Stibrany, Robert T., and Joseph A. Potenza. "rac-Dichlorido[3-ethoxy-3-(1-ethyl-1H-benzimidazol-2-yl)-2,3-dihydro-1H-pyrrolo[1,2-a]benzimidazole]copper(II)." Acta Crystallographica Section E Structure Reports Online 69, no. 2 (2013): m92—m93. http://dx.doi.org/10.1107/s1600536812051641.

Full text

Abstract:

The title complex, [CuCl2(C21H22N4O)], contains a bis(benzimidazole) unit with a chiral bridgehead C atom that forms part of a tetrahydropyrrole ring fused to one of the benzimidazoles. The chelate angle is 90.45 (9)° and the dihedral angle between the essentially planar benzimidazole fragments is 26.68 (9)°. The CuIIcoordination geometry lies approximately midway between tetrahedral and square planar. Overall, each chiral molecule contains six fused rings, and a racemic mixture is formed with symmetry-related enantiomers. In the crystal, C—H...π and C—H...Cl interactions link molecules into a

APA, Harvard, Vancouver, ISO, and other styles

4

H., E. MASTER, and R. KAMATH J. "Preparation of Newer Fused Benzimidazoles." Journal of Indian Chemical Society Vol. 72, Sep 1995 (1995): 645–46. https://doi.org/10.5281/zenodo.5909671.

Full text

Abstract:

Nadkamy-Sacasa Research Laboratory, St Xavier's College, Bombay-400 001 <em>Manuscript received 3 August 1993, revised 27 January 1994, accepted 8 February 1994</em> Preparation of Newer Fused Benzimidazoles.

APA, Harvard, Vancouver, ISO, and other styles

5

Bansal, Yogita, Manjinder Kaur, and Gulshan Bansal. "Antimicrobial Potential of Benzimidazole Derived Molecules." Mini-Reviews in Medicinal Chemistry 19, no. 8 (2019): 624–46. http://dx.doi.org/10.2174/1389557517666171101104024.

Full text

Abstract:

Structural resemblance of benzimidazole nucleus with purine nucleus in nucleotides makes benzimidazole derivatives attractive ligands to interact with biopolymers of a living system. The most prominent benzimidazole compound in nature is N-ribosyldimethylbenzimidazole, which serves as an axial ligand for cobalt in vitamin B12. This structural similarity prompted medicinal chemists across the globe to synthesize a variety of benzimidazole derivatives and to screen those for various biological activities, such as anticancer, hormone antagonist, antiviral, anti-HIV, anthelmintic, antiprotozoal, a

APA, Harvard, Vancouver, ISO, and other styles

6

Kapoor, Kamal, Parthasarathi Das, Rajni Khajuria, Sk Rasheed, and Chhavi Khajuria. "Recent Developments in the Synthesis of Pyrido[1,2-a]benzimidazoles." Synthesis 50, no. 11 (2018): 2131–49. http://dx.doi.org/10.1055/s-0036-1589533.

Full text

Abstract:

Pyrido[1,2-a]benzimidazole is one of the most important azaheterocyclic compounds consisting of three fused aromatic rings. Molecules containing this core have displayed a wide range of applications in the field of medicinal chemistry. The synthesis of pyrido[1,2-a]benzimidazole and its derivatives has attracted organic chemists because of its tremendous utility in interdisciplinary branches of chemistry. In this context, this review discusses the main advances in the synthesis of pyrido[1,2-a]benzimidazoles via metal-mediated and metal-free reactions from 2000 to 2016.1 Introduction2 Syntheti

APA, Harvard, Vancouver, ISO, and other styles

7

Sonawane, Amol D., Rohini A. Sonawane, Khin Myat Noe Win, Masayuki Ninomiya, and Mamoru Koketsu. "In situ air oxidation and photophysical studies of isoquinoline-fused N-heteroacenes." Organic & Biomolecular Chemistry 18, no. 11 (2020): 2129–38. http://dx.doi.org/10.1039/d0ob00375a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

MASTER, H. E., and J. R. KAMATH. "ChemInform Abstract: Preparation of Newer Fused Benzimidazoles." ChemInform 27, no. 50 (2010): no. http://dx.doi.org/10.1002/chin.199650172.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Qin, Hui, Yuanyuan Miao, Jian Xu, et al. "A facile and efficient [4 + 2] annulation reaction of sulfur ylides: access to N-fused benzimidazoles." Organic Chemistry Frontiers 6, no. 2 (2019): 205–8. http://dx.doi.org/10.1039/c8qo01133h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Nguyen, T. B., L. Ermolenko, and A. Al-Mourabit. "Formic acid as a sustainable and complementary reductant: an approach to fused benzimidazoles by molecular iodine-catalyzed reductive redox cyclization of o-nitro-t-anilines." Green Chemistry 18, no. 10 (2016): 2966–70. http://dx.doi.org/10.1039/c6gc00902f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

Kumar, Rajnish, Chanchal Singh, Avijit Mazumder, et al. "Synthetic Approach to Potential Anticancer Benzimidazole Derivatives: A Review." Mini-Reviews in Medicinal Chemistry 22, no. 9 (2022): 1289–304. http://dx.doi.org/10.2174/1389557521666211001122118.

Full text

Abstract:

Abstract: Cancer is one of the deadliest diseases in many developed and developing countries. Continuous efforts are required for designing better therapeutic agents for the treatment of cancer with more efficacy, selectivity, and less toxicity. The fused heterocyclic ring system has been identified by several researchers as a privileged structure that can be used as the basis for drug discovery in medicinal chemistry. The hetero-aromatic bicyclic ring system acts as a pharmacophore in a wide range of drugs with therapeutic potential. According to studies in the literature, various substituted

APA, Harvard, Vancouver, ISO, and other styles

12

Nandwana, Nitesh Kumar, Kasiviswanadharaju Pericherla, Pinku Kaswan, and Anil Kumar. "Synthesis of novel azole-fused quinazolines via one-pot, sequential Ullmann-type coupling and intramolecular dehydrogenative C–N bonding." Organic & Biomolecular Chemistry 13, no. 10 (2015): 2947–50. http://dx.doi.org/10.1039/c4ob02375g.

Full text

Abstract:

An efficient one-pot sequential procedure is described for the synthesis of novel azole-fused quinazolines through Ullmann-type coupling followed by cross dehydrogenative coupling of various azoles with 2-(2-bromophenyl)-1H-imidazole/benzimidazoles.

APA, Harvard, Vancouver, ISO, and other styles

13

Yang, Byeong Woo, Son Long Ho, Ho-Jin Lim, and Chan Sik Cho. "Palladium-catalyzed carbonylative cyclization of 2-(2-bromovinyl)benzimidazoles leading to pyrrolone-fused benzimidazoles." Journal of Organometallic Chemistry 806 (March 2016): 83–87. http://dx.doi.org/10.1016/j.jorganchem.2015.12.040.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Hsu, Wei-Shun, Min-Huan Tsai, Indrajeet J. Barve, Gorakh S. Yellol, and Chung-Ming Sun. "Synthesis of Aminofuran-Linked Benzimidazoles and Cyanopyrrole-Fused Benzimidazoles by Condition-Based Skeletal Divergence." ACS Combinatorial Science 19, no. 7 (2017): 492–99. http://dx.doi.org/10.1021/acscombsci.7b00052.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Nihar, Ranjan Kar, Samathoti Prasanthi, Muralitharan S., et al. "CURRENT TRENDS, MODERN SYNTHETIC APPROACH, SAR AND BIOLOGICAL ACTIVITIES OF BENZIMIDAZOLE DERIVATIVES." COMMUNITY PRACTITIONER 20, no. 09 (2023): 6–21. https://doi.org/10.5281/zenodo.8339770.

Full text

Abstract:

<strong>Abstract</strong> <strong>Background:</strong> Benzimidazole is a heterocyclic compound with a benzene ring fused to an imidazole ring. It is commercially available as a white, odorless, and tasteless powder. O-phenylenediamine and formic acid are condensed to form benzimidazole. The most common benzimidazole substance found in nature is N- riosyldimethylbenzimidazole, which functions as an axial ligand for cobalt in vitamin B12. <strong>Aim:</strong> The main objective of the review is to explore Current trends, modern synthetic approach, SAR and Biological activities of benzimid

APA, Harvard, Vancouver, ISO, and other styles

16

Dao, Pham Duy Quang, Ho-Jin Lim, and Chan Sik Cho. "Transition metal-free construction of trinuclear N-fused hybrid scaffolds by double nucleophilic aromatic substitution under microwave irradiation." Green Chemistry 21, no. 24 (2019): 6590–93. http://dx.doi.org/10.1039/c9gc03410b.

Full text

Abstract:

A green construction of trinuclear N-fused hybrid scaffolds by transition metal-free double C(sp<sup>2</sup>)–N coupling of 2-(2-bromoaryl)- and 2-(2-bromovinyl)benzimidazoles with 2-aminoazoles under microwave irradiation has been developed.

APA, Harvard, Vancouver, ISO, and other styles

17

Verma, Smita, Vishnuvardh Ravichandiran, Nihar Ranjan, and Swaran J. S. Flora. "Recent Advances in Therapeutic Applications of Bisbenzimidazoles." Medicinal Chemistry 16, no. 4 (2020): 454–86. http://dx.doi.org/10.2174/1573406415666190416120801.

Full text

Abstract:

Nitrogen-containing heterocycles are one of the most common structural motifs in approximately 80% of the marketed drugs. Of these, benzimidazoles analogues are known to elicit a wide spectrum of pharmaceutical activities such as anticancer, antibacterial, antiparasitic, antiviral, antifungal as well as chemosensor effect. Based on the benzimidazole core fused heterocyclic compounds, crescent-shaped bisbenzimidazoles were developed which provided an early breakthrough in the sequence-specific DNA recognition. Over the years, a number of functional variations in the bisbenzimidazole core have l

APA, Harvard, Vancouver, ISO, and other styles

18

Twardy, Dylan J., Kraig A. Wheeler, Béla Török, and Roman Dembinski. "Recent Advances in the Synthesis of Isoquinoline-Fused Benzimidazoles." Molecules 27, no. 7 (2022): 2062. http://dx.doi.org/10.3390/molecules27072062.

Full text

Abstract:

This review includes recent developments in the synthesis of benzo[4,5]imidazo[2,1-a]isoquinolines with particular attention given to categorizing protocols based on the structural features of the ring architecture and crystallographically characterized reaction products.

APA, Harvard, Vancouver, ISO, and other styles

19

Zhang, Xu, Yu Zhou, Hengshuai Wang, et al. "An Effective Synthetic Entry to Fused Benzimidazoles via Iodocyclization." Advanced Synthesis & Catalysis 353, no. 9 (2011): 1429–37. http://dx.doi.org/10.1002/adsc.201100038.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Aldabbagh, Fawaz, Joanne O’Connell, and Eoin Moriarty. "Access to Aromatic Ring-Fused Benzimidazoles Using Photochemical Substitutions of the Benzimidazol-2-yl Radical." Synthesis 44, no. 21 (2012): 3371–77. http://dx.doi.org/10.1055/s-0032-1316775.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Shen, Jianzhong, Jing Tong, Haiyang Jiang, et al. "Simultaneous Determination of Five Benzimidazoles in Feeds Using High-Performance Capillary Electrophoresis." Journal of AOAC INTERNATIONAL 92, no. 4 (2009): 1009–15. http://dx.doi.org/10.1093/jaoac/92.4.1009.

Full text

Abstract:

Abstract A high-performance capillary electrophoretic method for determination of five benzimidazoles (thiabendazole, albendazole, fenbendazole, mebendazole, oxfendazole) in animal feeds was developed. Separation was carried out in an 80.5 cm 75 m id fused-silica uncoated capillary and injected by hydrodynamic injection (35 mbar 8 s) at a wavelength detection of 295 nm. The drugs were completely resolved in 50 mmol/L citric acid buffer (pH 1.9) with 30 kV at a temperature of 25C. Linear range was 180 g/mL; limits of detection for the analytes were less than 2 mg/kg; the overall recoveries for

APA, Harvard, Vancouver, ISO, and other styles

22

Gong, Weitao, Peng Gao, Gang Li, Hassan Mehdi, Guiling Ning, and Jingjie Yu. "Construction of fluorescence-tunable pyrido-fused benzimidazoles via direct intramolecular C–H amination under transition-metal-free conditions." RSC Adv. 4, no. 93 (2014): 51268–71. http://dx.doi.org/10.1039/c4ra08954e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

El Ella, Dalai Abou, Edith Gößnitzer, and Winfried Wendelin. "Synthesis and structural elucidation of pyrimido-[1,2-a]benzimidazoles and fused derivatives. i. dihydropyrimido[1,2-a]benzimidazoles." Journal of Heterocyclic Chemistry 33, no. 2 (1996): 373–82. http://dx.doi.org/10.1002/jhet.5570330228.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

O'Connell, Joanne M., Eoin Moriarty, and Fawaz Aldabbagh. "ChemInform Abstract: Access to Aromatic Ring-Fused Benzimidazoles Using Photochemical Substitutions of the Benzimidazol-2-yl Radical." ChemInform 44, no. 11 (2013): no. http://dx.doi.org/10.1002/chin.201311123.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Zaitseva, Yu V., D. O. Egorov, R. S. Begunov, and A. I. Khlopotinin. "Antibacterial and antibiofilm activity of polyfunctional benzimidazole derivatives." Acta Biomedica Scientifica 7, no. 3 (2022): 134–41. http://dx.doi.org/10.29413/abs.2022-7.3.14.

Full text

Abstract:

Introduction. Compounds based on fused imidazole derivatives can become the basis for the development of a new generation of clinical therapeutic agents for more effective treatment of resistant human bacterial infections. This requires research, including the design, synthesis, and screening of biologically active compounds of this group.The aim. To study the effect of polyfunctional benzimidazole derivatives on the survival of Escherichia coli AB1157 culture and its ability to form biofilms.Methods. The antibacterial activity of the studied compounds was evaluated using the serial dilution m

APA, Harvard, Vancouver, ISO, and other styles

26

Anastasiou, Despina, Hassan Chaouk, and W. Roy Jackson. "A metal catalysed route to benzimidazoles containing a fused alicyclic ring." Tetrahedron Letters 32, no. 22 (1991): 2499–500. http://dx.doi.org/10.1016/s0040-4039(00)74365-6.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Zhang, Xu, Yu Zhou, Hengshuai Wang, et al. "ChemInform Abstract: An Effective Synthetic Entry to Fused Benzimidazoles via Iodocyclization." ChemInform 42, no. 46 (2011): no. http://dx.doi.org/10.1002/chin.201146125.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Li, Bingnan, Shaoyu Mai, and Qiuling Song. "Synthesis of fused benzimidazoles via successive nucleophilic additions of benzimidazole derivatives to arynes under transition metal-free conditions." Organic Chemistry Frontiers 5, no. 10 (2018): 1639–42. http://dx.doi.org/10.1039/c8qo00251g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Amalraj, S. David, G. Harichandran, D. Bhakiaraj, and A. Amalorpavadoss. "A Facile Catalytic One-Pot Synthesis of Benzimidazole and Benzothiazole Compounds using Amberlite IRA 400-Cl Resin as Green Catalyst." Asian Journal of Chemistry 34, no. 7 (2022): 1644–52. http://dx.doi.org/10.14233/ajchem.2022.23595.

Full text

Abstract:

A series of pharmaceutically valuable functionalized fused heteroaromatic compounds such as benzimidazoles and benzothiazoles have been synthesized via catalytic cyclocondensation between 1,2-phenylenediamine or 2-aminothiophenol and aryl aldehydes at ambient conditions. The Amberlite IRA400-Cl resin have been proved to be an efficient green catalyst in this protocol. The salient features of this method are the mild condition, easy work-up, an excellent yield of product, green catalyst and reusability of the catalyst.

APA, Harvard, Vancouver, ISO, and other styles

30

Kuzʼmenko, T. A., L. N. Divaeva, and A. S. Morkovnik. "New Synthesis of peri-Fused Tetrahydro[1,3]diazepino[1,2-a]benzimidazoles from 1-Aroylmethyl-2-[(4-hydroxybutyl)amino]benzimidazoles." Russian Journal of Organic Chemistry 56, no. 10 (2020): 1728–32. http://dx.doi.org/10.1134/s1070428020100097.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Rao, Tentu Nageswara, Suliman Yousef AlOmar, Faheem Ahmed, et al. "Reusable Nano-Zirconia-Catalyzed Synthesis of Benzimidazoles and Their Antibacterial and Antifungal Activities." Molecules 26, no. 14 (2021): 4219. http://dx.doi.org/10.3390/molecules26144219.

Full text

Abstract:

In this article, a zirconia-based nano-catalyst (Nano-ZrO2), with intermolecular C-N bond formation for the synthesis of various benzimidazole-fused heterocycles in a concise method is reported. The robustness of this reaction is demonstrated by the synthesis of a series of benzimidazole drugs in a one-pot method. All synthesized materials were characterized using 1HNMR, 13CNMR, and LC-MS spectroscopy as well as microanalysis data. Furthermore, the synthesis of nano-ZrO2 was processed using a standard hydrothermal technique in pure form. The crystal structure of nano-ZrO2 and phase purity were

APA, Harvard, Vancouver, ISO, and other styles

32

Song, Gui-Ting, Shi-Qiang Li, Zhi-Wei Yang, et al. "Microwave-assisted synthesis of fused piperazine-benzimidazoles via a facile, one-pot procedure." Tetrahedron Letters 56, no. 31 (2015): 4616–18. http://dx.doi.org/10.1016/j.tetlet.2015.06.035.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Barve, Indrajeet J., Chan‐Yu Chen, Deepak B. Salunke, Wen‐Sheng Chung, and Chung‐Ming Sun. "Design and Synthesis of New Biprivileged Molecular Scaffolds: Indolo‐Fused Benzodiazepinyl/quinoxalinyl benzimidazoles." Chemistry – An Asian Journal 7, no. 7 (2012): 1684–90. http://dx.doi.org/10.1002/asia.201200121.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

ANASTASIOU, D., H. CHAOUK, and W. R. JACKSON. "ChemInform Abstract: A Metal Catalyzed Route to Benzimidazoles Containing a Fused Alicyclic Ring." ChemInform 23, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.199212166.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

ghareb, Nagat, Asmaa Atta, and Ranza Elrayess. "Synthesis and Molecular docking Investigations of Ring-Fused Benzimidazoles as Novel Acetylcholinsterase Inhibitors." Records of Pharmaceutical and Biomedical Sciences 7, no. 1 (2023): 115–24. http://dx.doi.org/10.21608/rpbs.2023.200519.1217.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Alfonso, María, Antonia Sola, Antonio Caballero, Alberto Tárraga, and Pedro Molina. "Heteroditopic ligands based on ferrocenyl benzimidazoles fused to an additional diaza heterocyclic ring system." Dalton Transactions, no. 43 (2009): 9653. http://dx.doi.org/10.1039/b915627e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Gößnitzer, Edith, and Winfried Wendelin. "Synthesis and Structure Elucidation of Pyrimidobenzimidazoles and Fused Derivatives III [1,2]. Decahydropyrimido[1,2- a ]benzimidazol-2-oles and Octahydropyrimido[1,2- a ]benzimidazoles." Monatshefte fuer Chemie/Chemical Monthly 132, no. 5 (2001): 607–24. http://dx.doi.org/10.1007/s007060170098.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Mishra, Manisha, Dylan Twardy, Clifford Ellstrom, Kraig A. Wheeler, Roman Dembinski, and Béla Török. "Catalyst-free ambient temperature synthesis of isoquinoline-fused benzimidazoles from 2-alkynylbenzaldehydes via alkyne hydroamination." Green Chemistry 21, no. 1 (2019): 99–108. http://dx.doi.org/10.1039/c8gc02520g.

Full text

Abstract:

An efficient environmentally benign route for the synthesis of benzimidazo[2,1-a]isoquinoline has been developed by reacting 2-ethynylbenzaldehyde and related substituted alkynylbenzaldehydes with variously substituted ortho-phenylenediamines and aliphatic amines in ethanol.

APA, Harvard, Vancouver, ISO, and other styles

39

Song, Gui-Ting, Shi-Qiang Li, Zhi-Wei Yang, et al. "ChemInform Abstract: Microwave-Assisted Synthesis of Fused Piperazine-Benzimidazoles via a Facile, One-Pot Procedure." ChemInform 46, no. 45 (2015): no. http://dx.doi.org/10.1002/chin.201545186.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Martin, Anthony, Diana Cheshmedzhieva, Valeria Palermo та ін. "On the regioselective molecular sieves-promoted oxidative three-component synthesis of fused-benzimidazoles from β-ketoesters". Comptes Rendus. Chimie 25, G1 (2022): 19–29. http://dx.doi.org/10.5802/crchim.137.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Zhang, Xu, Yu Zhou, Hengshuai Wang, et al. "Silver-catalyzed intramolecular hydroamination of alkynes in aqueous media: efficient and regioselective synthesis for fused benzimidazoles." Green Chem. 13, no. 2 (2011): 397–405. http://dx.doi.org/10.1039/c0gc00668h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Ouyang, Huang-Che, Ri-Yuan Tang, Ping Zhong, Xing-Guo Zhang, and Jin-Heng Li. "CuI/I2-Promoted Electrophilic Tandem Cyclization of 2-Ethynylbenzaldehydes withortho-Benzenediamines: Synthesis of Iodoisoquinoline-Fused Benzimidazoles." Journal of Organic Chemistry 76, no. 1 (2011): 223–28. http://dx.doi.org/10.1021/jo102060j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Begunov, Roman S., and Galina A. Ryzvanovich. "Synthesis of pyrido[1,2-a]benzimidazoles and other fused imidazole derivatives with a bridgehead nitrogen atom." Russian Chemical Reviews 82, no. 1 (2013): 77–97. http://dx.doi.org/10.1070/rc2013v082n01abeh004295.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Goessnitzer, Edith, and Winfried Wendelin. "ChemInform Abstract: Synthesis and Structure Elucidation of Pyrimidobenzimidazoles and Fused Derivatives. Part 3. Decahydropyrimido[1,2-a]benzimidazol-2-oles and Octahydropyrimido[1,2-a]benzimidazoles." ChemInform 32, no. 34 (2010): no. http://dx.doi.org/10.1002/chin.200134158.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Drinkwater, Nyssa, Hoan Vu, Kimberly M. Lovell, et al. "Fragment-based screening by X-ray crystallography, MS and isothermal titration calorimetry to identify PNMT (phenylethanolamine N-methyltransferase) inhibitors." Biochemical Journal 431, no. 1 (2010): 51–61. http://dx.doi.org/10.1042/bj20100651.

Full text

Abstract:

CNS (central nervous system) adrenaline (epinephrine) is implicated in a wide range of physiological and pathological conditions. PNMT (phenylethanolamine N-methyltransferase) catalyses the final step in the biosynthesis of adrenaline, the conversion of noradrenaline (norepinephrine) to adrenaline by methylation. To help elucidate the role of CNS adrenaline, and to develop potential drug leads, potent, selective and CNS-active inhibitors are required. The fragment screening approach has advantages over other lead discovery methods including high hit rates, more efficient hits and the ability t

APA, Harvard, Vancouver, ISO, and other styles

46

Anastasiou, Despina, Eva M. Campi, Hassan Chaouk, and W. Roy Jackson. "Synthesis of benzimidazoles containing a fused alicyclic ring by Rhodium - catalysed hydroformylation of N-alkenyl-1,2-diaminobenzenes." Tetrahedron 48, no. 36 (1992): 7467–78. http://dx.doi.org/10.1016/s0040-4020(01)90361-8.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Sweeney, Martin, Michael Gurry, Lee-Ann J. Keane, and Fawaz Aldabbagh. "Greener synthesis using hydrogen peroxide in ethyl acetate of alicyclic ring-fused benzimidazoles and anti-tumour benzimidazolequinones." Tetrahedron Letters 58, no. 36 (2017): 3565–67. http://dx.doi.org/10.1016/j.tetlet.2017.07.102.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Thummanagoti, Suman, Gorakh S. Yellol, and Chung-Ming Sun. "Microwave-Assisted Tandem Transformation on an Ionic-Liquid Support: Efficient Synthesis of Pyrrolo/Pyridobenzimidazolones and Isoindolinone-Fused Benzimidazoles." Chemistry - An Asian Journal 6, no. 9 (2011): 2471–80. http://dx.doi.org/10.1002/asia.201100277.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Begunov, R. S., and G. A. Ryzvanovich. "ChemInform Abstract: Synthesis of Pyrido[1,2-a]benzimidazoles and Other Fused Imidazole Derivatives with a Bridgehead Nitrogen Atom." ChemInform 44, no. 33 (2013): no. http://dx.doi.org/10.1002/chin.201333238.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Zhang, Xu, Yu Zhou, Hengshuai Wang, et al. "ChemInform Abstract: Silver-Catalyzed Intramolecular Hydroamination of Alkynes in Aqueous Media: Efficient and Regioselective Synthesis for Fused Benzimidazoles." ChemInform 42, no. 27 (2011): no. http://dx.doi.org/10.1002/chin.201127163.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!