Relevant bibliographies by topics / Phthalimide

Contents

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

Academic literature on the topic 'Phthalimide'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Phthalimide"

1

Zhao, Xue. "Synthesis and application of N-butyl substituted phthalimide disperse dyes." Textile Research Journal 89, no. 15 (2018): 3034–47. http://dx.doi.org/10.1177/0040517518805380.

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Three azo dyes were synthesized using N-butyl substituted phthalimides as diazo components. All of the synthesized intermediate derivatives and dyes were characterized by mass spectrometry, proton nuclear magnetic resonance, infrared (IR) and elemental analyses. Synthesized dyes were also evaluated for their dyeing behavior and fastness properties toward polyester fabric. The ultraviolet-visible absorption maxima of the dyes were observed in the range of 445–563 nm. Bromo and cyano substitutions at the 3- and/or 5- positions of the phthalimide ring resulted in hypsochromic and bathochromic shi
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Oksdath-Mansilla, Gabriela, Adrián A. Heredia, Juan E. Argüello, and Alicia B. Peñéñory. "Photochemistry of N-(selenoalkyl)-phthalimides. Formation of N, Se-heterocyclic systems." Photochemical & Photobiological Sciences 14, no. 4 (2015): 726–36. http://dx.doi.org/10.1039/c4pp00452c.

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A number of selenium heterocyclic derivatives are obtained upon direct or acetone-sensitized irradiation of a variety ofN-(selenomethyl)alkyl-phthalimides. The reaction proceeds by photoinduced intramolecular electron transfer between the Se atom and the phthalimide moiety.
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Gramage-Doria, Rafael, Yu-Chao Yuan, and Christian Bruneau. "Merging Transition-Metal Catalysis with Phthalimides: A New Entry to Useful Building Blocks." Synthesis 50, no. 21 (2018): 4216–28. http://dx.doi.org/10.1055/s-0037-1610282.

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Phthalimides have found their main application in organic synthesis as protecting groups for primary amines during the multistep synthesis of biologically relevant targets. On the other hand, phthalimide functionalization is rather challenging and it is traditionally associated with the use of over-stoichiometric amounts of environmentally hazardous reagents. In this short review, we describe and discuss how, in the last decades, transition-metal catalysts have provided useful organic building blocks after selective transformation of the phthalimide skeleton in a more efficient and sustainable
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Basu, Souradeep, Alexander H. Sandtorv, and David R. Stuart. "Imide arylation with aryl(TMP)iodonium tosylates." Beilstein Journal of Organic Chemistry 14 (May 11, 2018): 1034–38. http://dx.doi.org/10.3762/bjoc.14.90.

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Herein, we describe the synthesis of N-aryl phthalimides by metal-free coupling of potassium phthalimide with unsymmetrical aryl(TMP)iodonium tosylate salts. The aryl transfer from the iodonium moiety occurs under electronic control with the electron-rich trimethoxyphenyl group acting as a competent dummy ligand. The yields of N-aryl phthalimides are moderate to high and the coupling reaction is compatible with electron-deficient and sterically encumbered aryl groups.
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Hasaninejad, Alireza, Abdolkarim Zare, Ahmad Reza Moosavi-Zare, Fatemeh Khedri, Rahimeh Rahimi, and Ali Khalafi-Nezhad. "Cs2CO3/[bmim]Br as an Efficient, Green, and Reusable Catalytic System for the Synthesis of N-Alkyl Derivatives of Phthalimide under Mild Conditions." Research Letters in Organic Chemistry 2008 (December 18, 2008): 1–4. http://dx.doi.org/10.1155/2008/419054.

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Aza-conjugate addition of phthalimide to α,β-unsaturated esters efficiently achieves in the presence of catalytic amount of Cs2CO3 and ionic liquid 1-butyl-3-methylimidazolium bromide ([bmim]Br) under mild reaction conditions (70°C) to afford N-alkyl phthalimides in high yields and relatively short reaction times.
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Le, Zhang Gao, Tao Zhong, Zong Bo Xie, and Jiang Ping Xu. "Solvent-Free N-Alkylation of Phthalimide Catalyzed by Basic Ionic Liquids." Advanced Materials Research 233-235 (May 2011): 1431–34. http://dx.doi.org/10.4028/www.scientific.net/amr.233-235.1431.

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Solvent-freeN-alkylation of phthalimide with alkyl halides catalyzed by basic ionic liquids was developed in this conmmunication. With a comparative study, [Bmim]OH (1-butyl-3-methyl imidazolium hydroxide) exhibited the highest catalytic activity among the selected basic ionic liquids, which afforded a convenient, efficient and general protocol forN-alkyl phthalimides exclusively.
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Aly, A. A., H. M. Ammar, and A. A. Khalil. "Copolymerization Parameters of 2-(N-Phthalimido) ethyl Methacrylate with Different Vinyl Monomers." Material Science Research India 8, no. 1 (2011): 17–24. http://dx.doi.org/10.13005/msri/080103.

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2-(N-phthalimido)ethyl methacrylate was prepared by the reaction of methacrylic acid with N-(2-hydroxyethyl)phthalimide in presence of N,N?-dicyclohexylcarbodiimide. The monomer reactivity ratios for copolymerization reactions of 2-(N-phthalimido)ethyl methacrylate with methyl acrylate, ethyl acrylate, butyl acrylate and styrene, respectively, in solution with azobisisobutyronitrile (AIBN) as initiator, were estimated by nitrogen analysis. The structure of the copolymers was investigated by IR spectroscopy. The Q and e values for 2-(N-phthalimido)ethyl methacrylate were calculated. Some of the
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Luzzio, Frederick A., DeAnna Piatt Zacherl, and William D. Figg. "A facile scheme for phthalimide ⇌ phthalimidine conversion." Tetrahedron Letters 40, no. 11 (1999): 2087–90. http://dx.doi.org/10.1016/s0040-4039(99)00152-5.

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Jourdain, Isabelle, Michael Knorr, Tom Charenton, Carsten Strohmann, Jan-Lukas Kirchhoff та Mohamed Othman. "(µ2-η4-N-(2-Butynyl)phthalimide)(hexacarbonyl)dicobalt". Molbank 2023, № 1 (2023): M1545. http://dx.doi.org/10.3390/m1545.

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The reaction of [Co2(CO)8] with an equimolar amount of the internal alkyne N-(2-butynyl)phthalimide (1-Phthalimido-2-butyne) 1 in heptane solution yields the title compound [Co2(CO)6(µ-phthalimidoCH2C≡CMe)] 2. Compound 2 has been characterized using IR, 1H and 13C NMR spectroscopy; the tetrahedrane-type cluster framework has been ascertained using a single-crystal X-ray diffraction study performed at 100 K.
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Perveen, Shagufta, and Raha Orfali. "L-Proline-Catalyzed Synthesis of Phthalimide Derivatives and Evaluation of Their Antioxidant, Anti-Inflammatory, and Lipoxygenase Inhibition Activities." Journal of Chemistry 2018 (August 1, 2018): 1–6. http://dx.doi.org/10.1155/2018/5198325.

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A study was planned to synthesize the phthalimide derivatives as phthalimides have versatile biological activities. To synthesize the phthalimide derivatives, initially the reaction was optimized with various catalysts, and L-proline was found to be the best catalyst as it provided excellent yield. A series of phthalimide derivatives was synthesized by facile one-top reaction of phthalic acid with aryl amines under mild reaction conditions in the presence of L-proline as catalyst. Products were obtained in excellent yields and structurally characterized by 1H, 13C NMR, and mass spectral data.
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Dissertations / Theses on the topic "Phthalimide"

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Chen, Gaoyum. "Lanthanide complexes of phthalimide and phthalamate containing ligands : synthesis, photophysical properties and their potential applications." Thesis, London Metropolitan University, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.571268.

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Molecular sensors and switches have made important contributions to biomedical devices and molecular computational operations. There are numerous molecular designs using a fluorophore linked through a spacer group to a receptor(s), with a wide dynamic range, directional precision, target specificity, and molecular logic capability. Tb(III) and Eu(III) metal ions have natural luminescence lifetimes in the order of milliseconds. As a result they have been used as probes that allow discrimination between probe emission and background fluorescence using time- resolved techniques. Unfortunately the
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Zhao-Karger, Zhirong. "The first anionic thia-Fries rearrangement at arene tricarbonylchromium complexes and reactions of phthalimide tricarbonylchromium complexes." [S.l.] : [s.n.], 2006. http://deposit.ddb.de/cgi-bin/dokserv?idn=983769435.

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Wang, Zhengfang. "Thiol Protein/Peptide Modification by N-(Phenylseleno)phthalimide and Applications of Chemometrics in Organic Food Authentication." Ohio University / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1395159533.

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Manley-King, Clarina Ilara. "The synthesis and evaluation of phthalimide analogues as inhibitors of monoamine oxidase B / Clarina Ilara Manley-King." Thesis, North-West University, 2011. http://hdl.handle.net/10394/8506.

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Parkinson’s disease (PD) is a multifactorial neurodegenerative disease believed to be caused by a number of factors. This has made the successful treatment of the disease very difficult, as the underlying cause of degeneration is still unknown. Monoamine oxidase (MAO-B) inhibitors have been used in the treatment of PD. MAO-B is known to be involved in the catalytic oxidation of biogenic amines, a reaction which produces aldehydes and hydrogen peroxide as byproducts. Both these by-products can be toxic if not rapidly cleared. Inhibitors of MAO-B conserve the depleted supply of dopamine and also
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Molitor, Sabrina [Verfasser]. "Aromatische Carbonsäureimide und -diimide in Photoinduzierten Elektronentransfer-Prozessen: Photodecarboxylative Addition von Carboxylaten durch Phthalimide und Pyromellitdiimide / Sabrina Molitor." München : Verlag Dr. Hut, 2016. http://d-nb.info/1115550292/34.

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GOMES, Paulo André Teixeira de Moraes. "Planejamento estrutural, síntese e avaliação das propriedades farmacológicas de inéditas tiazolil-hidrazonas derivadas da ftalimida e da isatina." Universidade Federal de Pernambuco, 2016. https://repositorio.ufpe.br/handle/123456789/18462.

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Submitted by Irene Nascimento (irene.kessia@ufpe.br) on 2017-03-30T18:26:28Z No. of bitstreams: 2 license_rdf: 1232 bytes, checksum: 66e71c371cc565284e70f40736c94386 (MD5) TESE PAULO ANDRÉ.pdf: 12707088 bytes, checksum: 1ef366976f050b974da19aa9ed860831 (MD5)<br>Made available in DSpace on 2017-03-30T18:26:29Z (GMT). No. of bitstreams: 2 license_rdf: 1232 bytes, checksum: 66e71c371cc565284e70f40736c94386 (MD5) TESE PAULO ANDRÉ.pdf: 12707088 bytes, checksum: 1ef366976f050b974da19aa9ed860831 (MD5) Previous issue date: 2016-07-27<br>FACEPE<br>A identificação e utilização de estruturas priv
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Van, der Walt Mietha Magdalena. "Syntheses of sulfanylphthalimide and xanthine analogues and their evaluation as inhibitors of monoamine oxidase and as antagonists of adenosine receptors / Mietha Magdalena van der Walt." Thesis, North-West University, 2013. http://hdl.handle.net/10394/9537.

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Currently L-DOPA is the drug most commonly used for the treatment of Parkinson’s disease (PD). However, the long-term use of L-DOPA is associated with the development of motor fluctuations and dyskinesias. Treatment mainly addresses the dopaminergic features of the disease and leaves its progressive course unaffected. An optimal treatment would be a combination of both motor and non-motor symptom relief with neuroprotective properties. Two drug targets have attracted the attention for PD treatment, namely monoamine oxidase B (MAOB) and adenosine A2A receptors. MAO-B inhibitors enhance the elev
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Chiba, Diego Eidy. "Planejamento, síntese e avaliação biológica de novos derivados da série LAPDESF FTD-AO com potencial atividade no tratamento da Doença de Alzheimer /." Araraquara, 2019. http://hdl.handle.net/11449/183180.

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Orientador: Man Chin Chung<br>Resumo: A doença de Alzheimer (DA) é a principal e mais comum causa de demência senil, contribuindo com 50-75% dos casos diagnosticados. Nos países desenvolvidos, a DA é quarta causa de morte, ficando atrás somente de doenças cardiovasculares, câncer e acidente vascular cerebral. A projeção da Organização Mundial de Saúde (OMS) é que até 2050 o número de idosos aumente 21% no mundo. A DA é uma doença neurodegenerativa progressiva, na qual os pacientes diagnosticados mostram uma extensa perda de sinapses e neurônios no hipocampo e nos córtex frontal e temporal, com
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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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Romagnoli, Elia. "Iridium-catalyzed asymmetric hydrogenation of N-allyl phthalimides." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2019. http://amslaurea.unibo.it/17959/.

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The unprecedented iridium-catalyzed asymmetric hydrogenation of N-allyl phthalimides to afford enantioenriched chiral amines bearing a β-methyl is presented. Recently developed Ir-MaxPHOX are used as catalysts for this enantioselective transformation. The hydrogenation reaction has been studied in detail in order to find the optimal conditions. The mild reaction conditions and the feasibility of the removal of the phthalimido protecting group makes this process easily scalable and of interest for multiple synthetic applications.
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Books on the topic "Phthalimide"

1

Ziegler, Pascal. Untersuchungen zur Photophysik und Photochemie N-substituierter Phthalimide. [s.n.], 1986.

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

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Folpet Health and Safety Guide (Heath & Safety Guide). World Health Organization, 1992.

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Kluckert, Jörg-Thomas. Beeinflussung der Bindung von [3H]N-Methylscopolamin an muscarinischen Acetylcholin-Rezeptoren aus Herz und Gehirn von Meerschweinchen durch das Phthalimido-Derivat W 84 und andere Verbindungen. 1991.

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Book chapters on the topic "Phthalimide"

1

Gooch, Jan W. "N-(Trichloromethylthio) Phthalimide." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_12094.

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Cavitt, T. Brian, Brian Phillips, Charles E. Hoyle, Chau K. Nguyen, Viswanathan Kalyanaraman, and Sonny Jönsson. "Photoinitiation of Acrylates via Sensitized Phthalimide Derivatives." In ACS Symposium Series. American Chemical Society, 2003. http://dx.doi.org/10.1021/bk-2003-0847.ch004.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand complex of iron(III) with phthalimide and salicylaldoxime." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_186.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand complex of iron(III) with phthalimide and benzildioxime." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_188.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand complex of iron(III) with phthalimide and α-furildioxime." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_187.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand complex of iron(III) with phthalimide and pyridine-2-aldoxime." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_189.

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Jinger, Suman, and Jyoti Chaudhary. "Homopolymer, Copolymers, and Terpolymer Synthesis Via Esterification-Cum-Addition of N-Substituted Phthalimide with Acrylates: Studies on Influences of Macromolecule Compositions on Thermal and Microbial Performances." In Advances in Polymer Sciences and Technology. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-13-2568-7_20.

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Andronati, S. A., T. A. Voronina, V. M. Sava, G. M. Molodavkin, S. Yu Makan, and S. G. Soboleva. "Affinity for Both 5-HT1A- and D1-Receptors and Anxiolytic Activity of N-(Arylpiperazinylalkyl) Phthalimides." In Molecular Recognition and Inclusion. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5288-4_32.

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Cristófalo, A. E., H. O. Montenegro, M. E. Cano, M. L. Uhrig, and J. P. Colomer. "Synthesis of 2-Propynyl 2-Acetamido-sss3,4,6-Tri-O-Acetyl-2-Deoxy-1-Thio-β-d-Glucopyranoside, 2-Propynyl 3,4,6-Tri-O-Acetyl-2-Deoxy-2-Phthalimido-1-Thio-β-d-Glucopyranoside and Their 2-(2-Propynylox­yethoxy)ethyl Analogs." In Carbohydrate Chemistry. CRC Press, 2021. http://dx.doi.org/10.1201/9781351256087-27.

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McKeown, N. B. "From Phthalimide." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01843.

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Conference papers on the topic "Phthalimide"

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Zrilić, Sonja S., Jelena M. Živković, and Snežana D. Zarić. "Interaction energy and decomposition of interaction energy of halo-substituted phthalimide with carbon nanotube." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.666z.

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Interaction energy of phthalimide (ph) with carbon nanotube (CNT) calculated at SAPT0 level with a mixed basis set (6-31G* for CNT and 6-311G* for ph) is -19.51 kcal/mol. Halo-substitution of the phthalimide generally strengthens its interaction with the CNT and interaction energies are in the range from -21.02 kcal/mol to -22.62 kcal/mol going from ph-Cl to ph-I. However, interaction energy for phthalimide substituted with F atom (ph-F) is weaker (-18.81 kcal/mol) than for non-substituted phthalimide. For ph-Cl, ph-Br, ph-I, the total interaction energy increases with the higher halogen atomi
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Y.AL-BAITAI, Asmaa, Farah M.IBRAHIM, and Madeeha H. MAHMOOD. "ATOMISTIC SIMULATION STUDY ON THE CORROSION INHIBITION BY SOME PHTHALIMIDE DERIVATIVES." In IV.International Scientific Congress of Pure,Appliedand Technological Sciences. Rimar Academy, 2022. http://dx.doi.org/10.47832/minarcongress4-11.

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In this study, we used both the semi empirical PM3 and the molecular dynamics simulation methods based on the density functional theory to pursue an accurate description of the corrosion inhibition behavior of some phthalimide derivatives on the copper in the nitric acid solution which have been studied previously by another researchers work, via determine the relationship between the molecular structure of phthalimide derivatives and inhibition efficiency. Experimental work by using the weight loss method and polarization techniques suggests that these derivatives can be used a inhibitor. Fir
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Zrilić, Sonja S., Jelena M. Živković, and Snežana D. Zarić. "Influence of phthalimide substitution on the interaction with carbon nanotube." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.662z.

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The interaction energy of phthalimide and carbon nanotube calculated at SAPT0/6-31G* level is -17.37 kcal/mol. After the substitution of phthalimide with a hydroxyl group interaction was stronger (-18.64 kcal/mol) because of the larger dispersion followed by an increase in the molecular planar surface and an increased electrostatic term due to the additional electronegative oxygen atom. When a hexafluoroisopropyl group is used as a substituent (ph-6F/CNT), the molecule loses planarity and the dispersion term only slightly increases, but not enough to compensate for the unfavorable shift in the
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Winter, Georg E., Dennis L. Buckley, and James E. Bradner. "Abstract IA31: Phthalimide conjugation as a strategy for targeted protein degradation." In Abstracts: AACR Precision Medicine Series: Targeting the Vulnerabilities of Cancer; May 16-19, 2016; Miami, FL. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1557-3265.pmccavuln16-ia31.

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Mochizuki, H., and H. Tachibana. "Photoelectronic Properties of Thiophene-Vinylene Derivatives with Phthalimide Groups in Both Terminals." In 2017 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2017. http://dx.doi.org/10.7567/ssdm.2017.ps-10-05.

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Miquel-Leal, Francisco Javier, Natalia González-Zapata, Orlando José Jimenez-Jarava, et al. "Development and Optimization of the Multi-Gram Synthesis of the Antiviral 18-(Phthalimide-2-yl)ferruginol." In ECSOC-25. MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11667.

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Miquel-Leal, Francisco Javier, Natalia González-Zapata, Orlando José Jimenez-Jarava, et al. "Development and Optimization of the Multi-Gram Synthesis of the Antiviral 18-(Phthalimide-2-yl)ferruginol." In ECSOC-25. MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11667.

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Kumar, Rohitash, Ravindra Kumar, and Ambesh Dixit. "Thermal phase diagram of acetamide-benzoic acid and benzoic acid-phthalimide binary systems for solar thermal applications." In INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC 2015): Proceeding of International Conference on Condensed Matter and Applied Physics. Author(s), 2016. http://dx.doi.org/10.1063/1.4946738.

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Costantino, Andrea, Sandra Mandolesi, and Liliana Koll. "Michael Addition of Phthalimide and Saccharin to Enantiomerically Pure Diesters of BINOL and TADDOLs Derivatives Under Microwave Conditions." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-c012.

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Dekamin, Mohammad, Elham Ali та Mehrnoosh Ghanbari. "Quantitative Synthesis of α-Amino Nitriles through Strecker Reaction of Aldimines with TMSCN Catalyzed by Tetrabutylammonium phthalimide-N-oxyl". У The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00439.

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