Log in

Relevant bibliographies by topics / Phthalimidc

Contents

Journal articles
Dissertations / Theses
Books
Book chapters
Conference papers

Academic literature on the topic 'Phthalimidc'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Phthalimidc.'

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.

Journal articles on the topic "Phthalimidc"

1

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

2

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.

Full text

Abstract:

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.

APA, Harvard, Vancouver, ISO, and other styles

3

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.

Full text

Abstract:

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.

APA, Harvard, Vancouver, ISO, and other styles

4

Chetna, Ameta, Ameta Rakshit, Tiwari Urvashi, B. Punjabi P., and C. Ameta Suresh. "Enviro-economic synthesis of some phthalimide derivatives using microwave irradiation." Journal of Indian Chemical Society Vol. 88, Jun 2011 (2011): 827–33. https://doi.org/10.5281/zenodo.5770152.

Full text

Abstract:

Microwave Chemistry Laboratory, Department of Chemistry, Mohanlal Sukhadia University, Udaipur-313 001, Rajasthan, India <em>E-mail</em> : ameta_sc@yahoo.com Department of Pure and Applied Chemistry, University of Kota, Kota-324 005, Rajasthan. India <em>Manuscript received 14 June 2010, accepted 28 October 2010</em> An environmentally benign, efficient and facile route is developed for the preparation of phthalimide derhatives by using LiBr as a catalyst under solvent free condition and microwave exposure. In comparison to conventional synthesis involving tedious workup, excessive use of solv

APA, Harvard, Vancouver, ISO, and other styles

5

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.

Full text

Abstract:

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.

APA, Harvard, Vancouver, ISO, and other styles

6

Bogdan, Anca, Myroslav O. Vysotsky, and Volker Böhmer. "Selective Derivatization of Calix[4]arenes via Amino Groups Attached to the Wide Rim." Collection of Czechoslovak Chemical Communications 69, no. 5 (2004): 1009–26. http://dx.doi.org/10.1135/cccc20041009.

Full text

Abstract:

A new strategy is proposed for the synthesis of tetraether derivatives of calix[4]arenes bearing at the wide rim nitro and phthalimido groups in well defined positions. Since both groups are precursors of amino functions, calix[4]arenes substituted by different N-acylamino residues are easily available in four steps. The essential steps during the synthesis of the precursor consist in the protection of amino groups by the formation of their phthalimides followed by ipso-nitration of the remaining tert-butylphenol ether units. This nitration occurs without side reactions at the phthalimido subs

APA, Harvard, Vancouver, ISO, and other styles

7

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

8

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.

Full text

Abstract:

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.

APA, Harvard, Vancouver, ISO, and other styles

9

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.

Full text

Abstract:

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.

APA, Harvard, Vancouver, ISO, and other styles

10

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

More sources

Dissertations / Theses on the topic "Phthalimidc"

1

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

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Habib, Osama Mahmoud Ali [Verfasser]. "Tricarbonylchrom(O)-Komplexe von Phthalimids Derivaten / Osama Mahmoud Ali Habib." Hannover : Technische Informationsbibliothek und Universitätsbibliothek Hannover, 2010. http://d-nb.info/1004016247/34.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

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/.

Full text

Abstract:

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.

APA, Harvard, Vancouver, ISO, and other styles

4

Hanft, Sebastian [Verfasser]. "Phthalimid-Harnstoff-Konjugate als Fluoreszenzsensoren und chirale Template für [4+4]-Cycloadditionen / Sebastian Hanft." München : Verlag Dr. Hut, 2014. http://d-nb.info/1060587572/34.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Oelgemöller, Michael. "Photochemie von Phthalimiden photodecarboxylative Addition von Carboxylaten und PET-induzierte Makrocyclisierungen /." [S.l. : s.n.], 1999. http://deposit.ddb.de/cgi-bin/dokserv?idn=95974973X.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

7

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Zhang, Yu-Feng. "Selective Electrocatalytic reduction mediated by Sm(II) : Application to nitroarenes, sulfoxides and phthalimides." Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLS596/document.

Full text

Abstract:

Le SmI₂ en tant que réactif de transfert monoélectronique a été largement utilisé en chimie organique depuis les premiers travaux de Kagan. Cependant, la quantité stœchiométrique ou en excès de SmI₂ et d'additifs toxique tels que HMPA sont utilisés normalement pour améliorer la réactivité. De plus, à cause de sa sensibilité à l'oxygène, le stockage de la solution de SmI₂ dans le THF est difficile. Récemment, nous avons développé une nouvelle méthode électrocatalytique basée sur la régénération électrochimique de Sm²⁺. Par rapport à la réactivité du SmI₂ classique, notre approche utilise une qu

APA, Harvard, Vancouver, ISO, and other styles

10

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

More sources

Books on the topic "Phthalimidc"

1

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

Find full text

APA, Harvard, Vancouver, ISO, and other styles

2

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

Find full text

APA, Harvard, Vancouver, ISO, and other styles

3

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

Find full text

APA, Harvard, Vancouver, ISO, and other styles

4

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.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Phthalimidc"

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Phthalimidc"

1

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

2

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

3

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

4

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

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.

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!