Relevant bibliographies by topics / Pyridyl

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Pyridyl'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Pyridyl"

1

Ramle, Abdul Qaiyum, Sang Loon Tan, and Edward R. T. Tiekink. "Synthesis and Crystallographic Characterisation of Pyridyl- and Indoleninyl-Substituted Pyrimido[1,2-b]Indazoles." Crystals 12, no. 9 (2022): 1283. http://dx.doi.org/10.3390/cryst12091283.

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Pyridyl- and indoleninyl-substituted pyrimido[1,2-b]indazole were synthesised in good to high yields from the condensation reaction of 1,3-dialdehydes with 3-aminoindazoles. The structural features of the compounds were determined by NMR (1H, 13C and 19F), FT-IR and HR-MS. The spectroscopic assignments were confirmed by X-ray crystallography for two derivatives, i.e., 9-Bromo-3-(pyridin-4-yl)pyrimido[1,2-b]indazole (1b) and 10-Methoxy-3-(pyridin-4-yl)pyrimido[1,2-b]indazole (1c), which further provides support for significant delocalisation of π-electron density over the entire fused ring syst
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Katsuta, Nagisa, Akio Mishima, Akira Fuyuhiro, Shinya Hayami та Satoshi Kawata. "Bis[μ-3,5-bis(pyridin-2-yl)-1H-pyrazole]bis[dibromidoiron(III)]". Acta Crystallographica Section E Structure Reports Online 69, № 11 (2013): m574. http://dx.doi.org/10.1107/s1600536813026573.

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The title dinuclear complex, [Fe2Br4(C13H9N4)2], which lies on an inversion center, features two approximately planar bis(pyridin-2-yl)pyrazole (bpypz−) ligands [maximum deviation = 0.082 (3) Å] and four bromide ions. Each FeIIIion is octahedrally coordinated by four N atoms of two bpypz−ligands and two Br ions. π–π stacking interactions [centroid–centroid distances = 3.7004 (17)–4.0123 (18) Å] are observed between pyridyl and pyrazole rings, and between pyridyl and pyridyl rings of adjacent complex molecules.
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Andersen, Heidi Gade, David Kvaskoff, and Curt Wentrup. "Bisiminopropadienes R-N=C=C=C=N-R from Pyridopyrimidines." Australian Journal of Chemistry 65, no. 6 (2012): 686. http://dx.doi.org/10.1071/ch12039.

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Chlorination of the N,N′-di(2-pyridyl)malonamide 13a affords 2-chloro-8-methyl-4-(2-(4-picolinyl)imino-4H-pyrido[1,2-a]pyrimidine 17a. Flash vacuum thermolysis of 17a causes efficient ring opening to the valence-tautomeric ketenimine 18a/19a, elimination of HCl, and formation of the bis(4-methyl-2-pyridyl)iminopropadiene, R-N=C=C=C=N-R 20a.
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Li, Huan Huan, Hai Bin Chu, Ying Nan Chen, et al. "Effects of Acidity on Nitrogen-Heterocyclic Compounds with Rare Earth Coordination and the Structure of Protonated Phenanthroline." Advanced Materials Research 233-235 (May 2011): 2808–11. http://dx.doi.org/10.4028/www.scientific.net/amr.233-235.2808.

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2,3-bis(2-pyridyl)-5,6-dihydropyrazine and a protonated phenanthroline (Phen) have been synthesized and the structure of protonated Phen is established by X-ray diffraction single crystal structure analysis. The coordination reactions of Phen, 2,2'- bipyridine and 2,3-bis(2-pyridyl)-5,6-dihydropyrazine with rare earth ions in low pH have been studied. The results show that 2,3-bis(2-pyridyl)-5,6-dihydropyrazine is hydrolyzed to be 2,2’-pyridil and protonated ethylenediamine. Meanwhile, Phen combines with proton, which results that nitrogen atoms can not coordinate with rare earth ions. The mol
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Yousaf, Muhammad, Nathan J. Yutronkie, Raúl Castañeda, Jacob A. Klein, and Jaclyn Brusso. "Boratriazines: inducing luminescence through boron incorporation into a terpy-type framework." New J. Chem. 41, no. 20 (2017): 12218–24. http://dx.doi.org/10.1039/c7nj02462b.

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The synthesis and physicochemical properties of pyridyl and pyrimidyl functionalized 1,3,5,2-triazaborinines are reported, along with the Lewis acid–base adduct pyrimidine-2-carboximidamide trifluoroborane, which forms as a side product in the reaction with the pyrimidyl substituents.
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Reynolds, Todd M., Steven M. Berry, and Deborah C. Bebout. "Crystal structure and Hirshfeld surface analysis of {2-[bis(pyridin-2-ylmethyl)amino]ethane-1-thiolato}chloridocadmium(II)." Acta Crystallographica Section E Crystallographic Communications 80, no. 10 (2024): 1081–86. http://dx.doi.org/10.1107/s2056989024009198.

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The title compound, [Cd(C14H16N3S)Cl] or [CdLCl] (1), where LH = 2-[bis(pyridin-2-ylmethyl)amino]ethane-1-thiol, was prepared and structurally characterized. The Cd2+ complex crystallizes in P21/c with a distorted trigonal–bipyramidal metal coordination geometry. Supramolecular interactions in 1 include parallel offset face-to-face interactions between inversion-related pyridyl rings and potential hydrogen bonds with chlorine or sulfur as the acceptor. Additional cooperative pyridyl–pyridyl interactions with roughly 45° tilt angles and centroid–centroid distances of less than 5.5 Å likely also
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Halushchenko, Valeriia, Oleksandr Korovin, Natalya Rusakova, et al. "Crystal structure and supramolecular features of bis{ethyl 2-[1-methyl-3-(pyridin-2-yl)-1H-1,2,4-triazol-5-yl]acetate}trinitratolanthanum(III)." Acta Crystallographica Section E Crystallographic Communications 81, no. 7 (2025): 632–35. https://doi.org/10.1107/s2056989025005419.

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The title lanthanum(III) complex, [La(Et-MPTA)2(NO3)3] {where Et-MPTA is ethyl 2-[1-methyl-3-(pyridin-2-yl)-1H-1,2,4-triazol-5-yl]acetate} or [La(C24H28N8O4)(NO3)3], crystallizes in the monoclinic space group C2/c (No. 15). The lanthanum atom is twelve-coordinate, bonded to two oxygen atoms from carboxylate groups, four nitrogen atoms from two pyridinyl-1,2,4-triazole ligands, and six oxygen atoms of three NO3 − anions. The coordination geometry around the lanthanum atom can be described as a distorted icosahedron. Supramolecular features include π-stacking interactions between pyridyl and tri
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Tan, Sang Loon, Nathan R. Halcovitch, and Edward R. T. Tiekink. "N,N′-Bis(pyridin-4-ylmethyl)oxalamide benzene monosolvate: crystal structure, Hirshfeld surface analysis and computational study." Acta Crystallographica Section E Crystallographic Communications 75, no. 8 (2019): 1133–39. http://dx.doi.org/10.1107/s2056989019009551.

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The asymmetric unit of the title 1:1 solvate, C14H14N4O2·C6H6 [systematic name of the oxalamide molecule: N,N′-bis(pyridin-4-ylmethyl)ethanediamide], comprises a half molecule of each constituent as each is disposed about a centre of inversion. In the oxalamide molecule, the central C2N2O2 atoms are planar (r.m.s. deviation = 0.0006 Å). An intramolecular amide-N—H...O(amide) hydrogen bond is evident, which gives rise to an S(5) loop. Overall, the molecule adopts an antiperiplanar disposition of the pyridyl rings, and an orthogonal relationship is evident between the central plane and each term
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Laachir, Abdelhakim, Fouad Bentiss, Salaheddine Guesmi, Mohamed Saadi та Lahcen El Ammari. "Crystal structure of bis[2,5-bis(pyridin-2-yl)-1,3,4-thiadiazole-κ2N2,N3]bis(thiocyanato-κS)copper(II)". Acta Crystallographica Section E Crystallographic Communications 72, № 8 (2016): 1176–78. http://dx.doi.org/10.1107/s2056989016011713.

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The mononuclear title complex, [Cu(SCN)2(C12H8N4S)2], was obtained by the reaction of 2,5-bis(pyridin-2-yl)-1,3,4-thiadiazole and potassium thiocyanate with copper(II) chloride dihydrate. The copper cation lies on an inversion centre and displays an elongated octahedral coordination geometry. The equatorial positions are occupied by the N atoms of two 2,5-bis(pyridin-2-yl)-1,3,4-thiadiazole ligands, whereas the axial positions are occupied by the S atoms of two thiocyanate anions. The thiadiazole and the pyridyl rings linked to the metal are approximately coplanar, with a maximum deviation fro
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Karthikeyan, Iyyanar, Dhanarajan Arunprasath, and Govindasamy Sekar. "An efficient synthesis of pyrido[1,2-a]indoles through aza-Nazarov type cyclization." Chemical Communications 51, no. 9 (2015): 1701–4. http://dx.doi.org/10.1039/c4cc08783f.

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Transition metal free Brønsted acid mediated synthesis of pyrido[1,2-a]indole scaffolds has been developed through aza-Nazarov type cyclization of readily available diaryl(2-pyridyl)methanol using formic acid for the synthesis of biologically and medicinally important pyrido[1,2-a]indole, indolo[1,2-a]quinoline and pyrimido[1,2-a]indole derivatives.
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Dissertations / Theses on the topic "Pyridyl"

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Smith, Amy Elizabeth. "Functionalised pyridyl- and pyrimidyl-boronic acids and derived new biheteroaryls." Thesis, Durham University, 2005. http://etheses.dur.ac.uk/2751/.

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The novel substituted pyridylboronic acids 2-ethoxy-3-pyridylboronic acid 103, 2,6- dimethoxy-3-pyridylboronic acid 146, 2,3-dimethoxy-4-pyridylboronic acid 158, 2,6- difluoro-3-pyridylboronic acid 225, 2,6-dichloro-3-pyridylboronic acid 230 and 2,3- dichloro-4-pyridylboronic acid 238 have been synthesised, and the synthesis of existing alkoxy pyridylboronic acids 2-methoxy-5-pyridylboronic acid 40 and 2-methoxy-3- pyridylboronic acid 43 has been optimized and scaled up. The novel substituted pyrimidylboronic acids 2-chloro-5-pyrimidylboronic acid 244 and 2-amino-5- pyrimidylboronic acid 221 h
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Hargreaves, Christopher ? "Polyfluoro-pyridyl glycosyl donors." Thesis, Durham University, 2005. http://etheses.dur.ac.uk/2733/.

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Carbohydrates are one of the most structurally and functionally diverse classes of naturally occurring compounds and it is well established that they play an essential role in a vast array of biological processes. The synthesis of stereochemically defined oligosaccharides by a series of glycosylation processes, involving the reaction between a glycosyl donor and acceptor, is of paramount importance in synthetic carbohydrate chemistry and glycobiology. However, despite the importance of glycosylation chemistry and the development of sophisticated methodologies, there remains no general and ster
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Bullock, Thomas Hornsby. "Group 13 tris-pyridyl complexes." Thesis, University of Cambridge, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578971.

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Skelton, Lorraine Ann. "Pyridyl quinazolines as potential antitumour agents." Thesis, Institute of Cancer Research (University Of London), 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294789.

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Tabanella, Stefania. "Pyridyl-amino acids for potential catalysts." Thesis, University of Sheffield, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.269279.

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Yamaguchi, Shigeru. "Studies on Metallation of β-Pyridyl Porphyrins". 京都大学 (Kyoto University), 2011. http://hdl.handle.net/2433/142408.

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Smith, Dan Andrew. "N-phosphino-pyridyl imines : flexible, multi-functional reagents." Thesis, Durham University, 2009. http://etheses.dur.ac.uk/42/.

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Chapter I includes a summary of the chemistry of phosphines and bidentate phosphorus-nitrogen ligands of relevance to this thesis, and highlights their application in transition metal-based catalysis. In addition, a review of the characteristic properties and reactivity of iminophosphoranes and phosphenium cations is presented in preparation for work outlined later in this manuscript. The synthesis and coordination studies of a range of N-phosphino-pyridyl imines with the general structure (C5H5N)(Ar)C=NPR2 (1) {R = alkyl or aryl and Ar = aryl} are reported in chapter II. The molecular structu
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Rogers, Michael Charles. "Synthesis and reactivity of new tris-pyridyl complexes." Thesis, University of Cambridge, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.614195.

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Ahmed, Aminu. "Mixed donor carbene pyridyl ligands and their metal complexes." Thesis, Cardiff University, 2008. http://orca.cf.ac.uk/54889/.

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This thesis describes the synthesis of a series of Ag(I), Pd(II), Rh(I) and Ir(I) complexes of quinoline functionalised nucleophilic heterocyclic carbene (NHC) ligands. The transmetallation properties of the Ag(I) complexes were utilised to prepare the corresponding Pd(II), Rh (I) and Ir(I) (NHC) complexes. A series of quinoline based imidazolium, pyrimidinium salts were prepared and characterised as NHC ligand precursors. Ag(I)(NHC) complexes were prepared by the reaction of the quinoline functionalised salts with Ag20 in DCM. All complexes were spectroscopically characterised and the results
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McNally, C. T. "Transition metal complexes of pyridyl functionalized n-heterocyclic carbenes." Thesis, Queen's University Belfast, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.546329.

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Books on the topic "Pyridyl"

1

Sheldon, Philippa. Coordination chemistry of azamacrocycles functionalised with N-pendant pyridyl, bipyridyl and terpyridyl arms. typescript, 1994.

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Friesenegger, Susanne. Metabolismus von 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanon (NNK) in Gewebeschnitten von Syrischen Goldhamstern. [s.n.], 1999.

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M, Smith Stephen. Synthesis and molecular modelling of azamacrocycles and azacalix[3]arenes with N-pendant pyridyl and 2,2'-bipyridyl arms. typescript, 1996.

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Hamburg, Universität, ed. Antitumoraktive Pyrido[3,2-d]-1-benzazepine. [s.n.], 1996.

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Notholt, Justus. Untersuchungen zum oberflächenverstärkten Ramaneffekt im System Silber-Pyridin. A.S. Intemann und Ch.C. Intemann, 1988.

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Pfleiderer, Mathias. Synthese und Eigenschaften 6-substituierter Pyrido[2,3-d]pyrimidine. Hartung-Gorre, 1986.

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Rasor, Johann Peter. Zur Pyridin-katalysierten Umsetzung chiraler Alkohole mit [alpha]-Arylalkylessigsäureanhydriden [Alpha-Arylalkylessigsäureanhydriden]: Diastereoselektivität in Experiment und Modell. [s.n.], 1988.

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8

Al-Harbi, Ahmed Baker. Synthesis and Coordination Chemistry of Oxygen Rich Ligands: Bis(oxoimidazolyl)hydroborato, Tris(oxoimidazolyl)hydroborato and Tris(2-pyridonyl)methane. [publisher not identified], 2014.

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Sequeira, Pearl Astrid. Pyridyl(methyl)ketenes: Preparation, detection and trends in reactivity. 2004.

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Bauer, L., and S. Prachayasittkul. Review of Some Recent Syntheses, Reactions and Bioactivities of Pyridyl Sulfides. Gordon and Breach, 1987.

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Book chapters on the topic "Pyridyl"

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Canary, James W., Yihan Wang, Richard Roy, Lawrence Que, and Hiroyuki Miyake. "Tris[(2-Pyridyl)Methyl] Amine (TPA) and (+)-Bis[(2-Pyridyl)methyl]-1-(2-Pyridyl)-Ethylamine (α-Metpa)." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132630.ch11.

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Baker, Don R., Keith H. Brownell, Ian R. Matthews, and Paul Worthington. "Novel Class of Pyridyl Fungicides." In ACS Symposium Series. American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0584.ch037.

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Morgan, Michael M., MacDonald J. Christie, Thomas Steckler, et al. "(–)-1-Methyl-2-(3-Pyridyl)Pyrrolidine." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_3001.

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Li, Jie Jack, and Minmin Yang. "Pyridines—The Magic of Phenyl–Pyridyl Switch." In Drug Discovery with Privileged Building Blocks. CRC Press, 2021. http://dx.doi.org/10.1201/9781003190806-23.

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Butcher, Howard J., Everly B. Fleischer, E. L. Muetterties, E. J. Muetterties, and M. C. Muetterties. "α,β,γ,δ-Tetra(4-pyridyl)porphinezinc." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132432.ch45.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed-valence binuclear MnIV-MnIII complex with methyl[2-(2-pyridyl)ethyl] (2-pyridyl-methyl)amine)." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_711.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) α-formyl pyridyl hydrazine complex." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_395.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(III) α-formyl pyridyl hydrazone complex." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_175.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(III) α-acetyl pyridyl hydrazone complex." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_176.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(III) α-benzoyl pyridyl hydrazone complex." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_177.

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Conference papers on the topic "Pyridyl"

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Meyer, Kelly, Kyle Crabtree, Jasmine Keane, Anahut Sandhu, J. Westerfield, and Sommer Johansen. "ROTATIONAL SPECTROSCOPY OF PYRIDYL RADICALS." In 2020 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2020. http://dx.doi.org/10.15278/isms.2020.ti06.

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Meyer, Kelly, Kyle Crabtree, Jasmine Keane, Anahut Sandhu, J. Westerfield, and Sommer Johansen. "AB INITIO SPECTROSCOPIC PARAMETERS OF PYRIDYL RADICALS." In 2021 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2021. http://dx.doi.org/10.15278/isms.2021.wm06.

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Silva, Anderson B. da, and Juliana A. Vale. "Rapid synthesis of di-1,2,4-oxadiazoles pyridyl compounds." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0031-1.

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Silva, Anderson B. da, and Juliana A. Vale. "Rapid synthesis of di-1,2,4-oxadiazoles pyridyl compounds." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0317-1.

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Popusoi, Ana, Nicanor Barba, and Aurelian Gulea. "Synthesis of 1,3-Phenyl(Pyridyl)propenones with thiosemicarbazidic groups." In Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab03.

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The bibliographic study of chalcones of the type 1,3-aryl(heteryl)propen-2-one with thiosemicarbazidic 4- and 1,4-disubstituted and thisemicarbazonic groups respectively gives us the information that they have a wide spectrum of biological activity, but methods of their synthesis are less described in the literature, and they became our object of study. 4,5-Dihydro-1-H-(pyrazol-3-yl)phenylhydrazinecarbothioamides 3a and 3b were obtained according to the following scheme:Reagents and reaction conditions: i, ii) 2-Py, 25oC – 24h, 90-95oC – 3h, 77-82%; iii) DMF, CH3COOH, 70-80oC, 2-3h, 60-63%. Fi
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Barbosa, Luiz C. A., Carmindo R. Borel, Sergio A. Fernandes, and Célia R. A. Maltha. "Povarov reaction for the synthesis of 2-(2-pyridyl)quinoline." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013816161848.

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Andrejević, Tina P., Darko P. Ašanin, Nada D. Savić, Nevena Lj Stevanović, Miloš I. Djuran, and Biljana Đ. Glišić. "DNA/BSA BINDING STUDY OF DINUCLEAR GOLD(III) COMPLEXES WITH AROMATIC NITROGEN-CONTAINING HETEROCYCLES AS BRIDGING LIGANDS." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.312a.

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In recent decades, a special attention has been devoted to gold(III) complexes as potential antitumor agents due to their structural similarity to platinum(II) complexes. One of the possible mechanisms of the mode of antitumor activity of gold(III) complexes could include their interaction with DNA. However, the effectiveness of the therapeutic agents also depends on the degree of its binding to proteins present in the blood plasma, because, in this way, it is transported to the cell. Considering this, we investigated the interactions of three dinuclear gold(III) complexes of the general formu
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Meyer, P., and B. Czarnecki. "398. 1-(2-Pyridyl) Piperazine Stability on Coated Glass Fiber Filters." In AIHce 1996 - Health Care Industries Papers. AIHA, 1999. http://dx.doi.org/10.3320/1.2765077.

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Huang, Hongbing, Lisa Acquaviva, Howard Bregman та ін. "Abstract 1621: Discovery of pyridyl pyrrolopyridinones as potent and selective CK1γ inhibitors". У Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-1621.

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Savchuk, Maria I., Dmitry S. Kopchuk, Alexey P. Krinochkin, et al. "Preparation of indole-containing 3-(2-pyridyl)-1,2,4-triazines as tryptamine derivatives." In PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON AUTOMOTIVE INNOVATION GREEN ENERGY VEHICLE: AIGEV 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5087380.

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Reports on the topic "Pyridyl"

1

Jessen, S. W., J. W. Blatchford, Y. Z. Wang, D. D. Gebler, and L. B. Lin. Exciton Dynamics in Poly(p-pyridyl Vinylene). Defense Technical Information Center, 1996. http://dx.doi.org/10.21236/ada305228.

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Ram, M. S., and J. T. Hupp. Generalized Synthesis of cis- and trans-Dioxorhenium(V) (Bi)pyridyl Complexes. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada231829.

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Jessen, S. W., J. W. Blatchford, Y. Z. Wang, D. D. Gebler, and L. B. Lin. Direct and Photoinduced Absorption in Poly(p-pyridyl Vinylene): Morphological Control of Triplet Excitons and Polarons. Defense Technical Information Center, 1996. http://dx.doi.org/10.21236/ada305224.

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Wang, Chenyi. Spectroscopy, NMR, and Electrochemistry Studies of Protonated Aminophenyl/Pyridyl Porphyrins and Their Application in Hydrogen Evolution. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.2220.

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Zagorchev, Plamen, Elisaveta Apostolova, Vesela Kokova, Lyudmil Peychev, Zhivko Peychev, and Milena Draganova-Filipova. Activation of Kv7.2 to Kv7.5 Channels by Retigabine Modulates the Effects of Histamine and 2‑(2‑Pyridyl) Ethylamine on Smooth Muscles. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, 2018. http://dx.doi.org/10.7546/crabs.2018.10.18.

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