Log in

Relevant bibliographies by topics / 4,5-dihydro-1H-pyrazoles / Journal articles

To see the other types of publications on this topic, follow the link: 4,5-dihydro-1H-pyrazoles.

Journal articles on the topic '4,5-dihydro-1H-pyrazoles'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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 '4,5-dihydro-1H-pyrazoles.'

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

Zhu, Yu, Jun-Jie Hong, Yun-Bin Zhou, Yu-Wei Xiao, Min Lin, and Zhuang-Ping Zhan. "Selective synthesis of 4-(sulfonyl)-methyl-1H-pyrazoles and (E)-4,5-dihydro-1H-pyrazoles from N-allenic sulfonylhydrazones." Org. Biomol. Chem. 12, no. 23 (2014): 3797–801. http://dx.doi.org/10.1039/c4ob00550c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Kukharev, B. F., V. K. Stankevich, N. A. Lobanova, G. R. Klimenko, and E. Kh Sadykov. "N-(2-Vinyloxyethyl)-4,5-dihydro-1H-pyrazoles." Russian Journal of Organic Chemistry 43, no. 4 (2007): 628–29. http://dx.doi.org/10.1134/s1070428007040264.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Chovatia, P. T., J. D. Akabari, P. K. Kachhadia, P. D. Zalavadia, and H. S. Joshi. "Synthesis and selective antitubercular and antimicrobial inhibitory activity of 1-acetyl-3,5-diphenyl-4,5-dihydro-(1h)-pyrazole derivatives." Journal of the Serbian Chemical Society 71, no. 7 (2006): 713–20. http://dx.doi.org/10.2298/jsc0607713c.

Full text

Abstract:

The new compounds 1-aryl-3-{1-phenyl-3-[p (methylthio)phenyl]pyrazol-4-yl}-2-propen-1-ones 2a?l were prepared by the condensation of 1-phenyl-3-[p (methylthio)phenyl]-4-formylpyrazole 1 with different aryl ketones. Compounds 2a?l in reaction with hydrazine hydrate yielded 3-aryl-5-{1-phenyl-3-[p-(methylthio)phenyl]pyrazol-4 yl}-4,5-dihydro-(1H)-pyrazoles 3a?l and in the presence of hydrazine hydrate in glacial acetic acid gave 1-acetyl-3-aryl 5-{1-phenyl-3-[p-(methylthio)phenyl]pyrazol-4-yl}-4,5 dihydro-(1H)-pyrazoles 4a?l. These compounds were tested in vitro for their antitubercular and anti

APA, Harvard, Vancouver, ISO, and other styles

4

Thirunarayanan, Ganesamoorthy, and K. Ravi. "Synthesis and Spectral Correlation Study of some 3-(3,4-dichlorophenyl)-5-(Substituted Phenyl)-4,5-dihydro-¹H-Pyrazole-1-yl-Ethanones." International Letters of Chemistry, Physics and Astronomy 19 (October 2013): 44–57. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.19.44.

Full text

Abstract:

Some N-acetyl pyrazoles including 3-(3,4-dichlorophenyl)-5-(substituted phenyl)-4,5-dihydro-1H-pyrazole-1-yl-ethanones have been synthesised by solvent free cyclization cum acetylation of chalcones including substituted styryl 3,4-dichlorophenyl ketones using hydrazine hydrate and acetic anhydride in presence of catalytic amount of fly-ash: H2SO4 catalyst. The yield of these N-acetyl pyrazole derivatives are more than 75%. The synthesised N-acetyl pyrazoline derivatives were characterized by their physical constants and spectral data. The infrared spectral νC=N and C=O (cm-1) frequencies, NMR

APA, Harvard, Vancouver, ISO, and other styles

5

Chen, Yi-Hui, Hai-Tao Tang, Jia-Hao Zeng, Jun-Jia Chen, and Zhuang-Ping Zhan. "Synthesis of (E)-4,5-Dihydro-1H-Pyrazoles via Tandem Intermolecular Addition–Cyclization of N-Propargylic Sulfonylhydrazones." Synlett 28, no. 15 (2017): 2036–40. http://dx.doi.org/10.1055/s-0036-1588844.

Full text

Abstract:

A new strategy for the synthesis of (E)-4-benzylidene-4,5-dihydro-1H-pyrazoles through tandem intermolecular addition–intramolecular cyclization of N-propargylic sulfonylhydrazones has been developed. In this study, we firstly report that N-propargylic sulfonylhydrazones react with electrophilic reagents to afford 4-substituted pyrazole derivatives.

APA, Harvard, Vancouver, ISO, and other styles

6

Altıntop, Mehlika Dilek. "Synthesis, In vitro and In silico Evaluation of a Series of Pyrazolines as New Anticholinesterase Agents." Letters in Drug Design & Discovery 17, no. 5 (2020): 574–84. http://dx.doi.org/10.2174/1570180816666190618111023.

Full text

Abstract:

Background: Pyrazolines, electron-rich nitrogen carriers, are of great importance due to their potential applications for the treatment of many diseases including inflammation, infectious diseases and neurodegenerative disorders. Objectives: The purpose of this work was to synthesize new pyrazoline derivatives and evaluate their anticholinesterase effects. Methods: 1-Aryl-5-[4-(piperidin-1-yl)phenyl]-3-(3,4-dimethoxyphenyl)-4,5-dihydro-1H-pyrazoles (1-7) were synthesized via the treatment of 1-(3,4-dimethoxyphenyl)-3-[4-(piperidin-1-yl)phenyl]prop-2- en-1-one with arylhydrazine hydrochloride d

APA, Harvard, Vancouver, ISO, and other styles

7

Kukharev, B. F., V. K. Stankevich, N. A. Lobanova, V. G. Chernova, E. Kh Sadykov, and V. A. Apkhanov. "Reactions of vinyl 2,3-epoxypropyl ethers with 4,5-dihydro-1H-pyrazoles." Russian Journal of Organic Chemistry 42, no. 10 (2006): 1498–500. http://dx.doi.org/10.1134/s1070428006100174.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Burde, P. C., and A. M. Rahatgaonkar. "Facile Synthesis and Biological Evaluation of Cyclopropyl-Pyrazole Hybrids in [bmim][PF6]-Water Biphasic System as Antifungal Agents." Asian Journal of Organic & Medicinal Chemistry 4, no. 3 (2019): 152–58. http://dx.doi.org/10.14233/ajomc.2019.ajomc-p192.

Full text

Abstract:

3-Cyclopropyl-5-(4-substituted)-1-phenyl-4,5-dihydro-1H-pyrazoles derived from corresponding chalcones were synthesized and evaluated for their biological activities. A convenient synthesis of a library of these compounds in 1-butyl-3-methylimidazolium hexafluorophosphate-water biphasic system at ambient temperature has been accomplished. The ionic liquid, [bmim][PF6] and water which are immiscible, has been easily recycled and reused after separation of the products without any noticeable diminution in its activity.

APA, Harvard, Vancouver, ISO, and other styles

9

Venkata Narsimha Reddy, Chintalapani, Eligeti Rajanarendar, and Ananthula Krishnamurthy. "Synthesis of 3-methyl-1,5-diphenyl-7-aryl-7,8-dihydro-6H-pyrazolo[4,5-b]azepines." Collection of Czechoslovak Chemical Communications 55, no. 4 (1990): 1055–58. http://dx.doi.org/10.1135/cccc19901055.

Full text

Abstract:

3,5-Dimethyl-4-nitro-1-phenylpyrazole (I) on treatment with chalcones II under phase transfer conditions gives the Michael adducts, 3-methyl-4-nitro-1-phenyl-5-(2-aryl-4-phenyl-4-oxo-1-butyl)pyrazoles (III). The Michale adducts on cycloreduction with stannous chloride-hydrochloric acid furnish 3-methyl-1,5-diphenyl-7-aryl-7,8-dihydro-6H-pyrazolo[4,5-b]azepines (IV). IR, 1H NMR, 13C NMR and mass spectra support the structures of III and IV.

APA, Harvard, Vancouver, ISO, and other styles

10

Ramos, Daniela Fernandes, Gabriela Fiss, Clarissa Piccinin Frizzo, et al. "Activity of 4,5-dihydro-1H-pyrazoles against Mycobacterium tuberculosis and nontuberculous mycobacteria." International Journal of Antimicrobial Agents 43, no. 5 (2014): 481–83. http://dx.doi.org/10.1016/j.ijantimicag.2014.02.004.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

Zhu, Yu, Jun-Jie Hong, Yun-Bin Zhou, Yu-Wei Xiao, Min Lin, and Zhuang-Ping Zhan. "ChemInform Abstract: Selective Synthesis of 4-(Sulfonyl)-methyl-1H-pyrazoles and (E)-4,5-Dihydro-1H-pyrazoles from N-Allenic Sulfonylhydrazones." ChemInform 45, no. 44 (2014): no. http://dx.doi.org/10.1002/chin.201444124.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Pasin, J. S. M., A. P. O. Ferreira, A. L. L. Saraiva, et al. "Antipyretic and antioxidant activities of 5-trifluoromethyl-4,5-dihydro-1H-pyrazoles in rats." Brazilian Journal of Medical and Biological Research 43, no. 12 (2010): 1193–202. http://dx.doi.org/10.1590/s0100-879x2010007500139.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Odin, I. S., A. A. Golovanov, V. V. Bekin, and V. S. Pisareva. "Synthesis and Acylation of 3-Aryl-5-(2-phenylethynyl)-4,5-dihydro-1H-pyrazoles." Chemistry of Heterocyclic Compounds 49, no. 11 (2014): 1687–90. http://dx.doi.org/10.1007/s10593-014-1421-7.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Dorn, Helmut, and R�diger Ozegowski. "LINK Synthesis with 3-Hydroxy-1H-pyrazoles: 3-Carboxyisoalkyloxy-1H-pyrazoles - bicyclic acylpyrazolium salts and ?-Lactams - 3-Carboxyisoalkyloxy-4,5-dihydro-1H-pyrazol-5-ones." Journal f�r Praktische Chemie/Chemiker-Zeitung 340, no. 5 (1998): 437–49. http://dx.doi.org/10.1002/prac.19983400506.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Machado, Pablo, Fernanda A. Rosa, Marcelo Rossatto, et al. "Synthesis and structure of novel 4,5-dihydro-1H-pyrazoles: salicylic acid based analgesic agents." Arkivoc 2007, no. 16 (2008): 281–97. http://dx.doi.org/10.3998/ark.5550190.0008.g28.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Pizzuti, Lucas, Luciana A. Piovesan, Alex F. C. Flores, Frank H. Quina, and Claudio M. P. Pereira. "Environmentally friendly sonocatalysis promoted preparation of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro-1H-pyrazoles." Ultrasonics Sonochemistry 16, no. 6 (2009): 728–31. http://dx.doi.org/10.1016/j.ultsonch.2009.02.005.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Zhou, Zhixuan, Jiaru Zhuo, Sujun Yan, and Lin Ma. "Design and synthesis of 3,5-diaryl-4,5-dihydro-1H-pyrazoles as new tyrosinase inhibitors." Bioorganic & Medicinal Chemistry 21, no. 7 (2013): 2156–62. http://dx.doi.org/10.1016/j.bmc.2012.12.054.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Sviridova, L. A., A. N. Tavtorkin, N. A. Shalynina, et al. "Synthesis of 4,5-dihydro-1H-pyrazoles with chiral substituents at position 3 or 5." Russian Chemical Bulletin 64, no. 5 (2015): 1078–82. http://dx.doi.org/10.1007/s11172-015-0981-8.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Martins, Marcos A. P., Paulo H. Beck, Lilian Buriol, et al. "Evaluation of the synthesis of 1-(pentafluorophenyl)-4,5-dihydro-1H-pyrazoles using green metrics." Monatshefte für Chemie - Chemical Monthly 144, no. 7 (2013): 1043–50. http://dx.doi.org/10.1007/s00706-013-0930-x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Pang, Wan, Shifa Zhu, Huanfeng Jiang, and Shizheng Zhu. "A novel synthesis of 5-perfluorophenyl 4,5-dihydro-1H-pyrazoles in THF or water." Journal of Fluorine Chemistry 128, no. 11 (2007): 1379–84. http://dx.doi.org/10.1016/j.jfluchem.2007.06.010.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Bharathi, R. "In vitro and molecular docking studies of an antiinflammatory scaffold with human peroxiredoxin 5 and tyrosine kinase receptor." Bioinformation 16, no. 11 (2020): 929–36. http://dx.doi.org/10.6026/97320630016929.

Full text

Abstract:

A new series of 4-(3-(2-amino-3,5-dibromophenyl)-1-(4-substitutedbenzoyl)-4,5-dihydro-1H-pyrazol-5-yl)benzonitrile (4a-h) compounds were synthesized and evaluated for in-vitro anti-inflammatory activities. The spectral (IR, NMR) and elemental analyses data of the product indicated the formation of new pyrazoles 4a-h. Compound 4e exhibited potent anti-inflammatory property with 85.45 % inhibitions. This value was compared with standard diclofenac sodium. This data is explained using molecular docking analysis of receptor-ligand binding. These results demonstrated that pyrazole derivatives are p

APA, Harvard, Vancouver, ISO, and other styles

22

Khan, Khalid A., and Hassan M. Faidallah. "1-Substituted carbamoyl and thiocarbamoyl-4,5-dihydro-1H-pyrazoles as possible cytotoxic and antimicrobial agents." Journal of Enzyme Inhibition and Medicinal Chemistry 31, no. 4 (2015): 619–27. http://dx.doi.org/10.3109/14756366.2015.1057717.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Ratković, Zoran, Jovana Muškinja, Adrijana Burmudžija, et al. "Dehydrozingerone based 1-acetyl-5-aryl-4,5-dihydro-1H-pyrazoles: Synthesis, characterization and anticancer activity." Journal of Molecular Structure 1109 (April 2016): 82–88. http://dx.doi.org/10.1016/j.molstruc.2015.12.079.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

DILIDDO, D., L. BRUCHE, P. BRAVO, D. FAVRETTO, and P. TRALDI. "ChemInform Abstract: Electron-Impact Mass Spectrometry of Trifluoromethyl-Substituted 4,5- Dihydro-1H- and -3H-pyrazoles." ChemInform 24, no. 17 (2010): no. http://dx.doi.org/10.1002/chin.199317044.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Odin, I. S., A. A. Golovanov, V. V. Bekin, and V. S. Pisareva. "ChemInform Abstract: Synthesis and Acylation of 3-Aryl-5-(2-phenylethynyl)-4,5-dihydro-1H-pyrazoles." ChemInform 45, no. 24 (2014): no. http://dx.doi.org/10.1002/chin.201424133.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Moreira, Dayse N., Clarissa P. Frizzo, Kelvis Longhi, Nilo Zanatta, Helio G. Bonacorso, and Marcos A. P. Martins. "An efficient synthesis of 1-cyanoacetyl-5-halomethyl-4,5-dihydro-1H-pyrazoles in ionic liquid." Monatshefte für Chemie - Chemical Monthly 139, no. 9 (2008): 1049–54. http://dx.doi.org/10.1007/s00706-008-0874-8.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Sauzem, Patricia D., Gabriela da S. Sant'Anna, Pablo Machado, et al. "Effect of 5-trifluoromethyl-4,5-dihydro-1H-pyrazoles on chronic inflammatory pain model in rats." European Journal of Pharmacology 616, no. 1-3 (2009): 91–100. http://dx.doi.org/10.1016/j.ejphar.2009.06.008.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

DORN, H., та R. OZEGOWSKI. "ChemInform Abstract: LINK Synthesis with 3-Hydroxy-1H-pyrazoles: 3-Carboxyisoalkyloxy-1H-pyrazoles - Bicyclic Acylpyrazolium Salts and γ-Lactams - 3-Carboxyisoalkyloxy-4,5-dihydro-1H-pyrazol-5-ones." ChemInform 29, № 46 (2010): no. http://dx.doi.org/10.1002/chin.199846136.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Dhingra, Ashwani Kumar, Bhawna Chopra, Rameshwar Dass, and Sanjeev K. Mittal. "Synthesis and Anti-Inflammatory Activity of Some O-Propargylated-N-acetylpyrazole Derived from 1,3-Diarylpropenones." International Journal of Medicinal Chemistry 2016 (January 11, 2016): 1–6. http://dx.doi.org/10.1155/2016/3156593.

Full text

Abstract:

In search of novel effective potent therapeutic agents delivered by oral route for inflammation treatment, some novel O-propargylated-N-acetylpyrazole analogs (5a–j) were prepared by treating N-acetylpyrazole (4a–j) derived from 1,3-diarylpropenones (3a–j) with propargyl bromide. Claisen-Schmidt condensation of a series of substituted aryl ketones 1 and benzaldehydes 2 in glacial acetic acid afforded 1,3-diarylpropenones which on further treatment with hydrazine hydrate in acetic acid under reflux conditions afforded 1-acetyl-3,5-diaryl-4,5-dihydro(1H)pyrazoles (4a–j). The products were charac

APA, Harvard, Vancouver, ISO, and other styles

30

PALLEAPATI, Kishor, Venkata Ramana KANCHARLAPALLI, and Afzal Basha SHAIK. "Synthesis, characterization and antitubercular evaluation of some new isoxazole appended 1-carboxamido-4,5-dihydro-1H-pyrazoles." Journal of Research in Pharmacy 23, no. 2 (2019): 156–63. http://dx.doi.org/10.12991/jrp.2019.120.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Mitkidou, Sophia, Stelios Papadopoulos, Julia Stephanidou-Stephanatou, Aristides Terzis, and Demetrios Mentzafos. "Unusual reactions between some 1-aroyl-4,5-dihydro-4,4-dimethyl-5-methylene-1H-pyrazoles and ketenes." Journal of Organic Chemistry 55, no. 15 (1990): 4732–35. http://dx.doi.org/10.1021/jo00302a046.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Agre, Neha, Mihir Khambete, Arundhati Maitra, et al. "Exploration of 5‐(5‐nitrothiophen‐2‐yl)‐4,5‐dihydro‐1H‐pyrazoles as selective, multitargeted antimycobacterial agents." Chemical Biology & Drug Design 95, no. 1 (2019): 192–99. http://dx.doi.org/10.1111/cbdd.13624.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Mishra, Anu, Pratibha Rai, Yogesh K. Pandey, Jaya Singh, and Jagdamba Singh. "An Eco-Sustainable Synthetic Approach for 4,5-Dihydro-1H -pyrazoles via DBU Catalysis in Micellar Medium." ChemistrySelect 2, no. 34 (2017): 10979–83. http://dx.doi.org/10.1002/slct.201702400.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Haunert, Frank, Martin H. Bolli, Berthold Hinzen, and Steven V. Ley. "Clean three-step synthesis of 4,5-dihydro-1H-pyrazoles starting from alcohols using polymer supported reagents." Journal of the Chemical Society, Perkin Transactions 1, no. 15 (1998): 2235–38. http://dx.doi.org/10.1039/a803609h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Tessmann, Josiane Weber, Julieti Buss, Karine Rech Begnini, et al. "Antitumor potential of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro-1H-pyrazoles in human bladder cancer cells." Biomedicine & Pharmacotherapy 94 (October 2017): 37–46. http://dx.doi.org/10.1016/j.biopha.2017.07.060.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Vorozhtsov, N. I., A. G. Majouga, E. K. Beloglazkina, et al. "Copper(ii) complexes with 3-(2-pyridyl)-4,5-dihydro-1H-pyrazoles: synthesis, structural and electrochemical studies." Russian Chemical Bulletin 63, no. 3 (2014): 657–61. http://dx.doi.org/10.1007/s11172-014-0488-8.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Frizzo, Clarissa P., and et al et al. "ChemInform Abstract: Evaluation of the Synthesis of 1-(Pentafluorophenyl)-4,5-dihydro-1H-pyrazoles Using Green Metrics." ChemInform 44, no. 42 (2013): no. http://dx.doi.org/10.1002/chin.201342112.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Waldo, Jesse P., Saurabh Mehta, and Richard C. Larock. "Room Temperature ICl-Induced Dehydration/Iodination of 1-Acyl-5-hydroxy-4,5-dihydro-1H-pyrazoles. A Selective Route to Substituted 1-Acyl-4-iodo-1H-pyrazoles." Journal of Organic Chemistry 73, no. 17 (2008): 6666–70. http://dx.doi.org/10.1021/jo800789p.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Azarifar, Davood, and Azadeh Gharshasbi. "Microwave-promoted Aromatization of 1,3,5-trisubstituted 4,5-Dihydro-1H-pyrazoles by Calcium Hypochlorite under Solvent-free Conditions." HETEROCYCLES 68, no. 6 (2006): 1209. http://dx.doi.org/10.3987/com-06-10701.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Buriol, Lilian, Clarissa P. Frizzo, Dayse N. Moreira, et al. "An E-factor minimized solvent-free protocol for the preparation of 4,5-dihydro-5-(trifluoromethyl)-1H-pyrazoles." Monatshefte für Chemie - Chemical Monthly 142, no. 5 (2011): 515–20. http://dx.doi.org/10.1007/s00706-011-0464-z.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Ishchenko, Roman A., Irina Yu Kargapolova, Natalia А. Orlova, et al. "Polyfluorinated triphenyl-4,5-dihydro-1H-pyrazoles with dendroid arylsulfanyl moieties as donor blocks in donor-acceptor chromophores." Journal of Fluorine Chemistry 248 (August 2021): 109841. http://dx.doi.org/10.1016/j.jfluchem.2021.109841.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Azarifar, Davood, Elahe Nadimi, Ramin Ghorbani-Vaghei, and Behrooz Maleki. "Microwave-assisted oxidation of 1,3,5-trisubstituted 4,5-dihydro-1H-pyrazoles to the corresponding pyrazoles with poly(N,N′-dibromobenzene-1,3-disulfonamide-1,2-ethanediyl)." Mendeleev Communications 16, no. 6 (2006): 330–31. http://dx.doi.org/10.1070/mc2006v016n06abeh002421.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Papadopoulos, Stelios, and Julia Stephanidou-Stephanatou. "Notizen 1,3-Dipolar Cycloadditions of Benzonitrile Oxides to 1-Aroyl-4,5-dihydro-3,4,4-trimethyl-5-methylene-1H-pyrazoles." Liebigs Annalen der Chemie 1985, no. 8 (1985): 1697–703. http://dx.doi.org/10.1002/jlac.198519850815.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

MITKIDOU, S., S. PAPADOPOULOS, J. STEPHANIDOU-STEPHANATOU, A. TERZIS, and D. MENTZAFOS. "ChemInform Abstract: Unusual Reactions Between Some 1-Aroyl-4,5-dihydro-4,4-dimethyl-5- methylene-1H-pyrazoles and Ketenes." ChemInform 22, no. 1 (2010): no. http://dx.doi.org/10.1002/chin.199101184.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

HAUNERT, F., M. H. BOLLI, B. HINZEN, and S. V. LEY. "ChemInform Abstract: Clean Three-Step Synthesis of 4,5-Dihydro-1H-pyrazoles Starting from Alcohols Using Polymer Supported Reagents." ChemInform 29, no. 51 (2010): no. http://dx.doi.org/10.1002/chin.199851142.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Rodrigo, Eduardo, M. Belén Cid, Christian Roussel, et al. "A Proof of Concept: 2-Pyrazolines (4,5-Dihydro-1H-pyrazoles) Can Be Used as Organocatalysts via Iminium Activation." Letters in Organic Chemistry 13, no. 6 (2016): 414–19. http://dx.doi.org/10.2174/1570178613666160815163117.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Singh, Nisha, Naresh K. Sangwan, and Kuldip S. Dhindsa. "Synthesis and fungitoxic activity of 5-aryl-1-formyl-4,5-dihydro-3-(2-hydroxyphenyl)-1H-pyrazoles and their complexes." Pest Management Science 56, no. 3 (2000): 284–88. http://dx.doi.org/10.1002/(sici)1526-4998(200003)56:3<284::aid-ps128>3.0.co;2-m.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Buriol, Lilian, Clarissa P. Frizzo, Dayse N. Moreira, et al. "ChemInform Abstract: An E-Factor Minimized Solvent-Free Protocol for the Preparation of 4,5-Dihydro-5-(trifluoromethyl)-1H-pyrazoles." ChemInform 42, no. 38 (2011): no. http://dx.doi.org/10.1002/chin.201138118.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Fioravanti, Rossella, Nicoletta Desideri, Mariangela Biava, Luca Proietti Monaco, Laura Grammatica, and Matilde Yáñez. "Design, synthesis, and in vitro hMAO-B inhibitory evaluation of some 1-methyl-3,5-diphenyl-4,5-dihydro-1H-pyrazoles." Bioorganic & Medicinal Chemistry Letters 23, no. 18 (2013): 5128–30. http://dx.doi.org/10.1016/j.bmcl.2013.07.035.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Pathak, Vinay, Hardesh K. Maurya, Sandeep Sharma, Kishore K. Srivastava, and Atul Gupta. "Synthesis and biological evaluation of substituted 4,6-diarylpyrimidines and 3,5-diphenyl-4,5-dihydro-1H-pyrazoles as anti-tubercular agents." Bioorganic & Medicinal Chemistry Letters 24, no. 13 (2014): 2892–96. http://dx.doi.org/10.1016/j.bmcl.2014.04.094.

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!