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Relevant bibliographies by topics / Phthalazine

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Academic literature on the topic 'Phthalazine'

Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

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Journal articles on the topic "Phthalazine"

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Mourad, Asmaa Kamal, Abdelmoneim Abdelsalam Makhlouf, Ahmed Yousef Soliman, and Samar Ahmed Mohamed. "Phthalazines and phthalazine hybrids as antimicrobial agents: Synthesis and biological evaluation." Journal of Chemical Research 44, no. 1-2 (October 29, 2019): 31–41. http://dx.doi.org/10.1177/1747519819883840.

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Phthalazine and phthalazinone derivatives are important owing to their significant biological activities and pharmacological properties. Herein, a benzoic acid derivative (2), a benzoxazin-1-one derivative (3), and an oxophthalazin-2(1 H)-yl)acetohydrazide (13) are utilized as precursors to construct a novel series of phthalazinones bearing various valuable functional groups in excellent yields via several simple and promising approaches. Finally, the antimicrobial activity of the newly synthesized phthalazines is screened against different microbial strains; namely, Gram-negative and Gram-positive bacteria utilizing Amoxicillin as a standard drug.

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Wasfy, A. A. F. "Fused Heterocycles. Part I. Synthesis of Some Annelated 1,2,4-Triazole Systems from [4-(1H-Benzimidazol-2-yl)-Phthalazin-1-Yl]Hydrazine." Journal of Chemical Research 2003, no. 8 (August 2003): 457–58. http://dx.doi.org/10.3184/030823403103174786.

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Substituted 6-(1 H-benzimidazol-2-yl)-[1,2,4]triazolo[3,4- a]phthalazine derivatives containing alkyl, aryl, hydroxyl, mercapto, methylthio and formyl substituents at position 3 have been synthesised. Di-[6-(1 H-benzimidazol-2-yl)-3-[1,2,4]triazolo[3,4- a]phthalazin-3-yl]alkanes have been obtained by the use of dicarboxylic acids or their esters in the above condensations. Methylation reactions of the triazolo-phthalazine system are reported.

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Xu, Jing. "Research on Synthesis of Triazine Ring and its Isomerization." Applied Mechanics and Materials 686 (October 2014): 26–30. http://dx.doi.org/10.4028/www.scientific.net/amm.686.26.

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This paper designed and synthesized a series of different chain length of phthalonitrile-terminated oligo (phthalazinone imide), it has good water solubility, and can be under normal atmospheric pressure to form the s-triazine rings-containing thermosetting oligo (phthalazine imide). Compared with the traditional thermosetting resin, the resin has the advantages of high temperature resistance, high strength, flame retardant, resistance to chemical corrosion.

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Plasseraud, Laurent, Hélène Cattey, and Philippe Richard. "Self-assembly Through Non-coordinating Intermolecular Forces, Part 2 [1]. Synthesis, Crystal Structure and Packing of [Cu2(μ-phthalazine)3(phthalazine)2][CF3SO3]2." Zeitschrift für Naturforschung B 63, no. 10 (October 1, 2008): 1169–74. http://dx.doi.org/10.1515/znb-2008-1005.

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Abstract Treatment of the copper(I) trifluoromethanesulphonate toluene complex {[Cu(CF3SO3)]2 · C6H5Me} (1) with phthalazine (phtz, C8H6N2) in dichloromethane-acetonitrile solution yielded, via the bis(acetonitrile)tris(μ-phthalazine)dicopper(I) trifluoromethanesulphonate intermediate (2), the novel bis(phthalazine)tris(μ-phthalazine)dicopper(I) trifluoromethanesulphonate salt (3). Compound 3 was completely characterised and the molecular structure determined by single-crystal X-ray diffraction. Complex 3 crystallises in the monoclinic system, space group C2/c, with a = 26.9527(10), b = 10.9558(7), c = 19.2104(10) Å , β = 127.268(2)◦, V = 4514.3(4) Å3 and Z = 4. The copper(I) coordination geometry is tetrahedral, each copper centre being linked to four phthalazine molecules. Dicationic units of 3 which present an unusual paddle wheel-like shape constitute appropriate organometallic building blocks for the construction of a supramolecular solid-state architecture. The analysis of the packing of the molecules of 3 in the crystal revealed an unprecedented 2-dimensional network, resulting from intermolecular π-π and electrostatic interactions.

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Habibi, Davood, Nosratollah Mahmoudi, and Omid Marvi. "Green Procedure for the Synthesis of Phthalazino[2,3‐b]phthalazine‐5,7,12,14‐tetraones." Synthetic Communications 37, no. 18 (September 1, 2007): 3165–71. http://dx.doi.org/10.1080/00397910701545247.

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Habibi, Davood, Nosratollah Mahmoodi, and Omid Marvi. "Montmorillonite K-10 clay as reusable heterogeneous catalyst for the microwave-mediated solventless synthesis of phthalazinetetraones." Canadian Journal of Chemistry 85, no. 2 (February 1, 2007): 81–84. http://dx.doi.org/10.1139/v06-189.

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Different phthalazino[2,3-b]phthalazine-5,7,12,14-tetraones were synthesized in a simple and environmentally benign method from the reaction of some phthalic anhydrides with semicarbazide or thiosemicarbazide using montmorillonite K-10 clay as solid heterogeneous acidic catalyst and microwaves under solvent-free conditions in good yields and short reaction times. The present method has many obvious advantages compared with those reported in the literature, including high efficiency, higher yield, operational simplicity, environmental benignity, and the possibility of recycling the solid clay. The solid clay catalyst used in the first cycle of the reactions was successfully recovered and reused in the second cycle, showing a gradual decrease in activity.Key words: montmorillonite K-10 clay, microwave, solvent-free condition, phthalazinetetraones, semicarbazide, thiosemicarbazide.

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Çelik, Ömer, Semra İde, Mustafa Kurt, and Şenay Yurdakul. "Dichlorobis(phthalazine)zinc(II)." Acta Crystallographica Section E Structure Reports Online 60, no. 8 (July 17, 2004): m1134—m1136. http://dx.doi.org/10.1107/s1600536804016915.

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Cai, Mingjian. "5-Bromophthalazine hemihydrate." Acta Crystallographica Section E Structure Reports Online 68, no. 8 (July 10, 2012): o2421. http://dx.doi.org/10.1107/s1600536812030358.

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The title compound, C8H5BrN2·0.5H2O, is a phthalazine derivative synthesized from 3-bromobenzene-1,2-dicarbaldehyde and hydrazine. The molecule is essentially planar, the deviation from the mean plane of the phthalazine ring being 0.015 (3) Å. The O atom of the solvent water molecule is situated on a twofold rotation axis. In the crystal, O—H...N hydrogen bonds and short N...Br [2.980 (3) Å] contacts lead to the formation of a two-dimensional network parallel to (101).

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Soliman, Saied M., Raghdaa A. Massoud, Hessa H. Al-Rasheed, and Ayman El-Faham. "Molecular and Supramolecular Structures of Cd(II) Complexes with Hydralazine-Based Ligands; A New Example for Cyclization of Hydrazonophthalazine to Triazolophthalazine." Crystals 11, no. 7 (July 15, 2021): 823. http://dx.doi.org/10.3390/cryst11070823.

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Molecular and supramolecular structures of two polymeric and one trinuclear Cd(II) complex with hydralazine-type ligands were presented. Self-assembly of E-1-(2-(thiophen-2-ylmethylene)hydrazinyl)phthalazine (HL) and CdCl2 gave the 1D coordination polymer [Cd(H2L)Cl3]n*H2O, 1, in which the Cd(II) ion is hexa-coordinated with one cationic monodentate ligand (H2L+) and five chloride ions, two of them acting as connectors between Cd(II) centers, leading to the formation of a 1D coordination polymer along the a-direction. Using DFT calculations, the cationic ligand (H2L+) could be described as a protonated HL with an extra proton at the hydrazone moiety. Repeating the same reaction by heating under reflux conditions in the presence of 1 mL saturated aqueous KSCN solution, the ligand HL underwent cyclization to the corresponding [1,2,4]triazolo[3,4-a]phthalazine-3(2H)-thione (TPT) followed by the formation of [Cd(TPT)(SCN)2]n*H2O, 2, a 1D coordination polymer. In this complex, the Cd(II) is coordinated with one NS-donor TPT bidentate chelate and two bridged μ(1,3)-thiocyanate ions connecting the Cd(II) centers forming the 1D polymer array along the b-direction. Heating E-2-(1-(2-(phthalazin-1-yl)hydrazono)ethyl)phenol HLOH with CdCl2 under reflux condition gave the trinuclear complex [Cd3(Hydralazine)2(H2O)2Cl6], 3, indicating the hydrolysis of the hydrazonophthalazine ligand HLOH during the course of the reaction. Due to symmetry considerations, there are only two different Cd(II) centers having CdN2Cl3O and CdN2Cl4 coordination environments. Hirshfeld topology analysis was used to analyze the solid-state supramolecular structure of the studied complexes.

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Çelik, Ömer, Semra İde, Mustafa Kurt, and Şenay Yurdakul. "Dibromobis(phthalazine-κN2)zinc(II)." Acta Crystallographica Section E Structure Reports Online 60, no. 4 (March 20, 2004): m424—m425. http://dx.doi.org/10.1107/s1600536804004908.

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Dissertations / Theses on the topic "Phthalazine"

1

Sheppard, Christopher Lorenzo. "Magnetostructural correlations in polynuclear complexes of phthalazine-based tetra- and hexadentate ligands." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ34227.pdf.

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Li, Jiyang [Verfasser]. "Investigation of Phthalazine, Quinazoline and Pyrimidine Derivatives as ABCG2 Inhibitors / Jiyang Li." Bonn : Universitäts- und Landesbibliothek Bonn, 2018. http://d-nb.info/1167857135/34.

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Kuzelka, Jane 1975. "Modeling the active sites of diiron and dicopper metalloproteins with napthyridine-, phthalazine-, and diethynylbenzene-based ligands." Thesis, Massachusetts Institute of Technology, 2003. http://hdl.handle.net/1721.1/30016.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2003.
Vita.
Includes bibliographical references.
Chapter 1. Bio-Inspired Reactions of Diiron Centers with Dioxygen A variety of biological systems employ carboxylate-bridged diiron centers to achieve substrate oxidation using dioxygen, and numerous small molecule model compounds have been synthesized in order to mimic this chemistry in the absence of a protein scaffold. In this introductory chapter, a brief overview is presented of ligand systems that have been used to prepare diiron complexes, and the subsequent oxidation chemistry of these systems is outlined. Chapter 2. Carboxylate, Phosphodiester, and Hydroxide-Bridged Diiron(II) Complexes with a Sterically Hindered Phthalazine Ligand The synthesis and crystallographic characterization of a series of diiron(II) complexes with a sterically hindered bridging phthalazine ligand are presented. The compounds [Fe₂(Ph₄bdptz)([mu]-O₂CR)₂]²⁺ (R = CH₃ (3); C₂H₅ (4); CH₂Ph (5); t-C₄H₉ (6)), [Fe₂(Ph₄bdptz)([mu]-O₂P(OPh)₂)₂]²⁺ (7), and [Fe₂(Ph₄bdptz) ([mu]-OH)(MeCN)₂]³⁺ (8) were prepared as small molecule models of the catalytic sites in non-heme carboxylate-bridged diiron enzymes. The phenyl rings of Ph4bdptz form a hydrophobic size-constrained pocket in which additional ligands can be accommodated, and they block the possible formation of tetranuclear species. As the steric bulk of the ancillary ligands is increased, the carboxylates shift from a syn, anti to a syn, syn coordination mode, and the Mossbauer spectra of the diiron(II) compounds clearly reflect the symmetry of the iron coordination environment. The oxidation chemistry of the diiron(II) compounds is presented.
(cont.) Chapter 3. Modeling Features of the Non-Heme Diiron Cores in O0-Activating Enzymes through the Synthesis, Characterization, and Oxidation of 1,8-Naphthyridine-Based Complexes Multidentate naphthyridine-based ligands were used to prepare a series of diiron(II) complexes. The compounds [Fe₂(BPMAN)([mu]-O₂CPh)₂](OTf)₂ (1), [Fe₂(BPMAN)([mu]-OR) ([mu]-0₂CAr[superscript]Tol)] (OTf)2 (R = H (2); CH₃ (3)), [Fe₂(BBAN)([mu]-0₂CAr[superscript]Tol)₃]-(OTf) (4), and [Fe₂(BEAN) ([mu]-O₂CAr[superscript]Tol)₃](OTf) (5) were prepared as models of the active sites of non-heme diiron enzymes. The rigorously enforced dinuclear core allows the reactivity of the diiron unit to be evaluated. Upon oxidation of these compounds, there is evidence for the formation of a ([mu]-oxo)diiron(III) unit, a mixed-valent ([mu]-oxo)Fe(II)Fe(III) species, and oxidative N-dealkylation. The electrochemical properties of the compounds were correlated with the observed dioxygen reactivity, and Mossbauer spectroscopic properties of the diiron(II) complexes were also investigated. Chapter 4. Modeling the Syn Disposition of Nitrogen Donors at the Active Sites of Carboxylate-Bridged Diiron Enzymes. Enforcing Dinuclearity and Kinetic Stability with a 1,2-Diethynylbenzene-Based Ligand The syn coordination of histidine residues at the active sites of several carboxylate-rich non-heme diiron enzymes has not been effectively reproduced with small molecule model compounds. In this study, ligands derived from 1,8- naphthyridine, phthalazine, and 1,2-diethynylbenzene were employed to mimic this geometric feature ...
by Jane Kuzelka.
Ph.D.

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Alzahrani, Nada Saleh. "The Synthesis and Characterization of the Bis-Substituted Phthalazine Using Bis-Substituted Isoindoline as Starting Material and Their Metals Complexes &The Synthesis and Charectrization of the Schiff Base Ligands with a Variety of Metals." University of Akron / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=akron1408102563.

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Houghton, Ralph Warren. "Synthesis of 1-substituted phenyl phthalazines." Scholarly Commons, 1990. https://scholarlycommons.pacific.edu/uop_etds/2201.

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The purpose of this work was the preparation of a new class of arylhydrazone reagents. When combined with a mixture of ketones and aldehydes, these new reagents would give derivatives different from those given by current arylhydrazone reagents. These derivatives could be separated by crystallization or chromatography and could then be easily characterized by x-ray crystallography or nuclear magnetic resonance (NMR).

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6

Ragunathan, Ramanaranjinie. "Studies of certain benzimidazoles, phthalazines and phthalimides." Thesis, Brunel University, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.292494.

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7

Johnsen, Matthias. "Neue Antithrombotika mit Phthalazin- und Pyridazin-Partialstrukturen." [S.l.] : [s.n.], 2002. http://www.diss.fu-berlin.de/2002/257/index.html.

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8

Jožef, Mađari. "Sinteza, strukturna, fizičko-hemijska i biološka karakterizacija novih N-heterocikličnih liganada i njihovih kompleksa sa jonima prelaznih metala." Phd thesis, Univerzitet u Novom Sadu, Prirodno-matematički fakultet u Novom Sadu, 2018. https://www.cris.uns.ac.rs/record.jsf?recordId=107656&source=NDLTD&language=en.

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Opisane su sinteze novih liganada bis(ftalazin-1hidrazon)-2,6-diacetilpiridna (Hz₂DAP·2HCl), bis(3-hlorpiridazin-6-hidrazon)-2,6-diacetilpiridina (Hp₂DAP), 3-hlorpiridazin-6-hidrazon di(2-piridil) ketona (HpDPK), ftalazin-1-hidrazon di(2-piridil)ketona (HzDPK) i ftalazin-1-hidrazon piridin-2-karbaldehida (HzPY). Zajedničko svojstvo dobijenih liganada je što sadrže piridinski i diazinski prsten i sadrže samo donorne atome azota. Tokom nastajanja kompleksa dolazi do deprotonacije liganada. Svi ligandi su okarakterisani elementalnom analizom, termoanalitičkim metodama i metodom IR spektroskopije, dok neki i metodom NMR spektroskopije kao i rendgenskom strukturnom analizom.Za sintezu koordinacionih jedinjenja primenjeni soli Co(II), Ni(II), Cu(II) i Zn(II). Dobijeni kompleksi su okarakterisani elementalnom analizom, konduktomerijskim i magnetnim merenjima, IR spektroskopijom i termoanalitičkim metodama. Barem jedan kompleks iz svake serije je okarakterisan i rendgenskom strukturnom analizom. Urađena su i ispitivanja antimikrobne aktivnosti odabranih jedinjenja prema predstavnicima grampozitivnih i gram-negativnih bakterija i kulturu kvasca. Pored toga, urađena su i ispitivanja citotoksične,antiproliferativne i inhibitorne aktivnosti jedinjenja prema roditeljskim i multirezistentnim T-limfomnim ćelijama kancera. Utvrđeno je da neka jedinjenja pokazuju izrazito mikrobicidno, citotoksično, antiproliferativno i inhibitorno dejstvo.
The synthesis of new ligands dihydrochloride salt of 2,6-diacetylpyridne bis(phthalazine-1hydrazone) (Hz₂DAP•2HCl), 2,6-diacetylpiridine bis(3- chloropyridazine-6-hydrazone) (Hp₂DAP), di(2-pyridyl)ketone 3-chloropyridazine- 6-hydrazone (HpDPK), di(2-pyridyl)ketone phthalazine-1-hydrazone (HzDPK) and pyridine-2-carbaldehide phthalazine-1-hydrazone (HzPY) have been described. All the ligands contain pyridine and diazine core and all of them have only nitrogen donor atoms. During the complex formation the deprotonation of ligands takes places. All of the ligands have been characterized by elemental analysis,thermoanalytical methods and IR spectroscopy. In some cases also by NMR spectroscopy and X-ray structural analysis.Co(II), Ni(II), Cu(II) and Zn(II) salts were used for the synthesis of the coordinational compounds. The obtained complexes were characterized by elemental analysis, molar conductivity and magnetic measurements, IR spectroscopy and thermoanalytical methods. At least one complex of each series were characterized by X-ray structural analysis.The antimicrobial activity of some of the compounds toward Gram-positive/Gram- negative bacteria furthermore, the cytotoxic, antiproliferative and inhibitory activity toward sensitive parental andmultiresistant T-lymphoma cancer cells have also been carried out. It can be concluded that some of the compounds exhibit outstanding antimicrobial, cytotoxic, antiproliferative, and inhibitory activity.

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Chang, Wen-Fu, and 張文福. "Phthalazine derivatives synthesize." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/37358420057208271610.

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碩士
國立中央大學
化學研究所
92
The heterocycles involving 1,4-dihydazinophthalazine (DHPH) as a building block have been paid considerable attention due to the significant biological applications. 1,4-dihydrazinophthalazine 1 reacted with 14、15 and 16. The ratio between 12 and 13, is dependent upon the pH of medium and temperature.1,4-dihydrazinophthalazine 1 reacted with aldehyde, followed by an oxidative cyclization to gave 22、28 and 29. When compound 29 was treated with 31 in ethanol under reflux for 12 h, it was also complex 32 .Upon irradiation with UV light, complex 32 changed color from yellow to red. The chemistry is yet to pursuit.

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Hung, Cheng-Lung, and 洪正龍. "Synthesis and Application of Ruthenium Complex Dyes Containing 1-(pyridin-2-yl)phthalazine Derivatives for Dye-sensitized Solar Cells (DSSCs)." Thesis, 2009. http://ndltd.ncl.edu.tw/handle/ynhygq.

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碩士
國立臺北科技大學
有機高分子研究所
97
Global environment concerns and the finite nature of fossil fuels have led to a growth of interest in the development of renewable energy. In order to maintain social and economic development, the solar energy is one of the best candidates of making a suitable transition to renewable fuels. Dye-sensitized solar cells (DSSCs) are currently attracting widespread interest for the conversion of sunlight into electricity because of their low cost and high efficiency. Charge separation is initiated at the dye, bound at the interface of an inorganic semiconductor like titanium dioxide and a holetransport material like the electrolyte. Careful design of the dye can minimize loss mechanisms and improve light harvesting. We synthesized new ruthenium(II) complex dyes containing novel ligands to improve the efficiency for DSSCs.

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Books on the topic "Phthalazine"

1

Brown, D. J. Cinnolines and Phthalazines. Hoboken, NJ, USA: John Wiley & Sons, Ltd, 2005. http://dx.doi.org/10.1002/0471744123.

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Cinnolines and phthalazines: Supplement 2. Hoboken, N.J: Wiley, 2005.

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Ragunathan, Ramanaranjinie. Studies of certain benzimidazoles, phthalazines and phthalimides. Uxbridge: Brunel University, 1991.

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Taylor, Edward C., Desmond J. Brown, and Jonathan A. Ellman. Cinnolines and Phthalazines, Supplement 2. Wiley & Sons, Incorporated, John, 2005.

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Castle, Raymond N. Condensed Pyridazines Including Cinnolines and Phthalazines. Wiley & Sons, Incorporated, John, 2009.

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Simpson, J. C. Pyridazine and Pyrazine Rings : (Cinnolines, Phthalazines, and Quinoxalines). Wiley & Sons, Incorporated, John, 2009.

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Taylor, Edward C., Peter Wipf, and Desmond J. Brown. Cinnolines and Phthalazines: Chemistry of Heterocyclic Compounds, Supplement II (Chemistry of Heterocyclic Compounds: A Series Of Monographs). Wiley-Interscience, 2005.

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Book chapters on the topic "Phthalazine"

1

Horkel, Ernst. "Metalation of Pyridazine, Cinnoline, and Phthalazine." In Topics in Heterocyclic Chemistry, 223–68. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/7081_2012_97.

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Winkelmann, Jochen. "Diffusion coefficient of 1,4-diphenylbenzo[g]phthalazine in tetrahydro-furan-d8." In Diffusion in Gases, Liquids and Electrolytes, 1200. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_976.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of hexanuclear copper(II) chloro complex with glycerol phthalazine." In Magnetic Properties of Paramagnetic Compounds, 1087–88. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_611.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of hexanuclear copper(II) bromo complex with glycerol phthalazine." In Magnetic Properties of Paramagnetic Compounds, 1089–90. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_612.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of hexanuclear copper(II) nitrato complex with glycerol phthalazine." In Magnetic Properties of Paramagnetic Compounds, 1091–92. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_613.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of octanuclear copper(II) chloro complex with pentaerythritol phthalazine." In Magnetic Properties of Paramagnetic Compounds, 1096–97. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_616.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of octanuclear copper(II) bromo complex with pentaerythritol phthalazine." In Magnetic Properties of Paramagnetic Compounds, 1098–99. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_617.

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Patel, Natu R. "Phthalazines." In Chemistry of Heterocyclic Compounds: A Series Of Monographs, 323–760. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186978.ch2.

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Winkelmann, Jochen. "Diffusion coefficient of 1,4-diphenylbenzo[g]phthalazine ion(2-) in tetrahydro-furan-d8." In Diffusion in Gases, Liquids and Electrolytes, 1201. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_977.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of tetranuclear copper(II) complex with novel dendritic poly(phthalazine) ligand." In Magnetic Properties of Paramagnetic Compounds, 1057–58. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_596.

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Conference papers on the topic "Phthalazine"

1

Raposo, M., Ana Sampaio, and G. Kirsch. "Synthesis of 1-amino-4-(2´-thienyl)phthalazine Derivatives." In The 8th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2004. http://dx.doi.org/10.3390/ecsoc-8-01948.

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Raposo, M., and Sara Fernandes. "Synthesis and characterization of novel phthalazine based push-pull heterocyclic systems for DSSC." In The 19th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a020.

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Raposo, M., and Sara Fernandes. "Synthesis and characterization of novel thienyl-phthalazine based heterocyclic systems functionalized with (bi)thiophene moieties." In The 21st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04797.

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Andrejevic, Tina, Dusan Milivojevic, Darko Ašanin, Nevena Stevanović, Jasmina Nikodinovic-Runic, Miloš Djuran, and Biljana Glišić. "DNA/BSA binding affinities and <em>in vivo</em> toxicity of dinuclear silver(I) complexes with phthalazine." In 6th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07371.

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Chen, Tai-Lin, Vicky Jain, Yi-Wen Lin, Tsann-Long Su, and Te-Chang Lee. "Abstract 3852: Development of1,2-bis(hydroxymethyl)benzo[g]pyrrolo[2,1-a]phthalazine hybrids as potent anticancer agents to small cell lung cancer." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-3852.

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Chen, Tai-Lin, Vicky Jain, Yi-Wen Lin, Tsann-Long Su, and Te-Chang Lee. "Abstract 3852: Development of1,2-bis(hydroxymethyl)benzo[g]pyrrolo[2,1-a]phthalazine hybrids as potent anticancer agents to small cell lung cancer." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-3852.

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Chen, Tai-Lin, Vicky Jain, Anilkumar S. Patel, Yi-Wen Lin, Tsann-Long Su, and Te-Chang Lee. "Abstract A002: Discovery of bis(hydroxymethyl)benzopyrrolo[2,1-a]phthalazine derivatives as orally bioavailable antitumor agents with anti-angiogenic and DNA cross-linking activities." In Abstracts: AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics; October 26-30, 2019; Boston, MA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1535-7163.targ-19-a002.

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Leng, Xiaohui, Yiming Wang, and Fei Wang. "Sulfonation of Poly(phthalazinone ether ketone) for MEMS humidity sensor." In 2018 IEEE Micro Electro Mechanical Systems (MEMS). IEEE, 2018. http://dx.doi.org/10.1109/memsys.2018.8346605.

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Yuan, Kuanyu, Cheng Liu, Hongmin Duan, Manxia Zhang, and Xigao Jian. "Preparation and Characterization of the Phthalazinone Structure-based Microporous Organic Polymer." In 2015 International Conference on Materials, Environmental and Biological Engineering. Paris, France: Atlantis Press, 2015. http://dx.doi.org/10.2991/mebe-15.2015.200.

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El Rayes, Samir, Ibrahim Ali, hamdy Abd Elazeem, and Sara Eltorky. "Convenient Synthesis of Some Novel 4-Benzyl-1(2H)-Phthalazinone Derivatives of expected anticancer activity." In The 23rd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2019. http://dx.doi.org/10.3390/ecsoc-23-06605.

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