Relevant bibliographies by topics / Iodo-compounds

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

Academic literature on the topic 'Iodo-compounds'

Author: Grafiati
Published: 5 June 2025
Last updated: 24 June 2025

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Journal articles on the topic "Iodo-compounds"

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Abdel Hamid, S., H. El-Obeid, K. Al-Rashood, A. Khalil, and H. El-Subbagh. "Substituted Quinazolines, 1. Synthesis and Antitumor Activity of Certain Substituted 2-Mercapto-4(3H)-quinazolinone Analogs." Scientia Pharmaceutica 69, no. 4 (2001): 351–66. http://dx.doi.org/10.3797/scipharm.aut-01-205.

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A new series of 4(3H)-quinazolinone analogs bearing 6-iodo and 2-thioether functions were synthesized and screened for their in vitro antitumor activity. Eight compounds were identified as active anticancer agents. 2-Mercapto-3-benzyl-4-thioxo-6-iodo-3H-quinazolin (2) and 2-(2,4-dinitrophenyl)-3-benzyl-6-iodo-4-(3H)-quinazolinone(9) proved to be the most active compounds in this study. They showed MG-MID GI50, TGI, LC50 values of 3.9, 25.2, 82.3 and 2.7, 12.3, 38.7 μM, respectively. The detailed synthesis and biological screening data are reported.
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2

Kumar, Rajesh, Nitya Sharma, and Om Prakash. "Hypervalent Iodine Reagents in the Synthesis of Flavonoids and Related Compounds." Current Organic Chemistry 24, no. 18 (2020): 2031–47. http://dx.doi.org/10.2174/1385272824999200420074551.

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Hypervalent iodine compounds have proved to be very useful reagents to bring about various oxidative transformations including (i) α-functionalization of carbonyl compounds, (ii) oxidation of phenols, and (iii) oxidative rearrangement of ketones and α,β- unsaturated ketones. These reactions find interesting applications in the development of newer and convenient approaches for the synthesis of flavonoids. This review focuses on the use of most common three hypervalent compounds, namely iodobenzene diacetate, [hydroxy(tosyloxy)iodo]benzene, and [bis-trifluoroacetoxy(iodo)]benzene in the synthesis of cis/trans-3-hydroxyflavanones, 3-hydroxyflavones (flavonols), flavones, isoflavones and related compounds.
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Chamsi, Ousama, Eric Pinelli, Bruno Faucon, et al. "Effects of herbicide mixtures on freshwater microalgae with the potential effect of a safener." Annales de Limnologie - International Journal of Limnology 55 (2019): 3. http://dx.doi.org/10.1051/limn/2019002.

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Freshwater microalgae are primary producers and cosmopolitan species subjected to the effects of herbicides. In this work, the in vitro algal growth inhibitory effects of 11 agrochemicals (9 herbicides, 1 metabolite, and 1 safener) were quantified. Chemical compounds were applied singly and in specific mixtures. Three species were used in axenic condition: the green alga Desmodesmus subspicatus (Chodat), the diatoms Nitzschia palea (Kützing) W. Smith and Navicula pelliculosa (Kützing) Hilse. When exposed to single compounds, N. palea and N. pelliculosa were only sensitive to atrazine/desethylatrazine and the safener benoxacor (BE), respectively. D. subspicatus was equally sensitive to four herbicides including atrazine and its metabolite and significantly more sensitive to iodosulfuron-methyl-sodium (IODO). The mixture of these five compounds induced a significantly higher growth inhibition of about 1.5-fold than IODO alone, which could be attributed to the four other herbicides. The mixture of all compounds was twofold less toxic than IODO on D. subspicatus. A halogen atom is present in IODO as in the herbicides to which the safener BE − known to induce glutathione-S-transferases − is associated in agrochemical preparations. We then showed that IODO was less toxic when combined with non-toxic concentrations of BE. These results indicated that the toxicity of the most active herbicide studied was decreased by a non-herbicide compound present in agrochemical formulations of other herbicides. These results suggest the importance to take into account the chemistry and the mechanisms of action for each compound in a risk assessment approach of a complex mixture.
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Wu, Jinsheng, Xiaolong Li, Mingyu Yang, Yujie Gao, Qianru Lv, and Baohua Chen. "Convenient synthesis of ferrocene amines via Cu-catalyzed coupling reaction." Canadian Journal of Chemistry 86, no. 9 (2008): 871–74. http://dx.doi.org/10.1139/v08-096.

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An efficient copper-catalyzed Ullmann-type cross-coupling reaction without ligand of iodo-ferrocene with amines has been reported. In this process, a range of ferrocenyl amine compounds have been prepared in moderate to good yields.Key words: amines, iodo-ferrocene, cross-coupling, copper, Ullmann coupling.
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S, G. ABDEL-HAMIDE. "Synthesis of some New Heterocyclic Systems bearing 2-Phenyl-6-iodo-4(3H)-quinazolinon-3-yl Moiety as Antibacterial Agents." Journal of Indian Chemical Society Vol. 74, Aug 1997 (1997): 613–18. https://doi.org/10.5281/zenodo.5891302.

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Pharmaceutical Chemistry Department, Al-Azhar University, Cairo, Nasr City, Egypt <em>Manuscript received 6 March 1995, revised 18 March 1996, accepted 24 July 1996</em> A number of heterobicyclic systems bearing 2-phenyl-6-iodo-4(3<em>H</em>)-quinazolinon-3-yl moiety have been synthesised by interaction of 3- amino-2-phenyl-6-iodo-4(3<em>H</em>)-quinazolinone with bifunctional compounds followed by cyclisation in different media. Some of the compounds possess high activity aganist bacteria.
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Agafonova, Anastasiya V., Ilia A. Smetanin, Nikolai V. Rostovskii, Alexander F. Khlebnikov, and Mikhail S. Novikov. "Easy Access to 2-Fluoro- and 2-Iodo-2H-azirines via the Halex Reaction." Synthesis 51, no. 24 (2019): 4582–89. http://dx.doi.org/10.1055/s-0039-1690200.

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A simple gram-scale method for the preparation of esters and dialkylamides of 2-(fluoro/iodo)-2H-azirine-2-carboxylic acids via the halogen exchange (Halex) reaction of 2-bromo-substituted analogues is reported. The method operates with inexpensive and safe reagents­, Bu4NF and potassium iodide, providing high product yields. Alternatively, 2-fluoro-2H-azirine-2-carboxylates can be prepared from 2-iodo- and 2-chloro-analogues. The latter compounds can be obtained in practically quantitative yield by treating the 2-iodo- and 2-bromo-2H-azirine-2-carboxylic esters with Bu4NCl.
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Bacsa, Ildikó, Rebeka Jójárt, János Wölfling та ін. "Synthesis of novel 13α-estrone derivatives by Sonogashira coupling as potential 17β-HSD1 inhibitors". Beilstein Journal of Organic Chemistry 13 (30 червня 2017): 1303–9. http://dx.doi.org/10.3762/bjoc.13.126.

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Novel 13α-estrone derivatives were synthesized by Sonogashira coupling. Transformations of 2- or 4-iodo regioisomers of 13α-estrone and its 3-methyl ether were carried out under different conditions in a microwave reactor. The 2-iodo isomers were reacted with para-substituted phenylacetylenes using Pd(PPh3)4 as catalyst and CuI as a cocatalyst. Coupling reactions of 4-iodo derivatives could be achieved by changing the catalyst to Pd(PPh3)2Cl2. The product phenethynyl derivatives were partially or fully saturated. Compounds bearing a phenolic OH group furnished benzofurans under the conditions used for the partial saturation. The inhibitory effects of the compounds on human placental 17β-hydroxysteroid dehydrogenase type 1 isozyme (17β-HSD1) were investigated by an in vitro radiosubstrate incubation method. Certain 3-hydroxy-2-phenethynyl or -phenethyl derivatives proved to be potent 17β-HSD1 inhibitors, displaying submicromolar IC50 values.
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Rochon, F. D., and P. C. Kong. "Iodo-bridged complexes of platinum(II) and synthesis of cis mixed-amine platinum(II) compounds." Canadian Journal of Chemistry 64, no. 9 (1986): 1894–96. http://dx.doi.org/10.1139/v86-312.

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Iodo-bridged platinum(II) dimers, [Pt(L)I2]2 with ligands (L) containing nitrogen as the donor atom, have been synthesized from the reactions of cis-[Pt(L)2I2] with perchloric acid. The dimers can be cleaved in aqueous media by a second nitrogen ligand to produce isometrically pure cis-[Pt(L)(L′)I2].These compounds can finally be converted to the chloro or carboxylato compounds by precipitating the iodo ligands with a silver salt and adding KCl or a carboxylate salt. Several compounds of the types cis-[Pt(L)(L′)Cl2] and cis-[Pt(L)(L′)(dicarboxylate)] were thus prepared. A few dimers of the type [(L)(L′)Pt(tetra-carboxylate)Pt(L)(L′)] were also synthesized.
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Glidewell, Christopher, John N. Low, Janet M. S. Skakle, Solange M. S. V. Wardell та James L. Wardell. "Isomeric iodo-N-(nitrobenzyl)anilines: interplay of hard and soft hydrogen bonds, iodo...nitro interactions and aromatic π...π stacking interactions". Acta Crystallographica Section B Structural Science 60, № 4 (2004): 472–80. http://dx.doi.org/10.1107/s0108768104012017.

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Molecules of 2-iodo-N-(4-nitrobenzyl)aniline, 4-O2NC6H4CH2NHC6H4I-2′ (1) are linked into chains by C—H...O hydrogen bonds. In the isomeric compound 3-iodo-N-(4-nitrobenzyl)aniline (2) a combination of N—H...O and C—H...O hydrogen bonds and iodo...nitro and aromatic π...π stacking interactions links the molecules into a three-dimensional framework structure. The two-dimensional supramolecular structure of 4-iodo-N-(4-nitrobenzyl)aniline (6) is built from a combination of C—H...O and N—H...π(arene) hydrogen bonds and aromatic π...π stacking interactions. 2-Iodo-N-(2-nitrobenzyl)aniline (7) crystallizes with two molecules in the asymmetric unit and these molecules are linked into ladders by a combination of N—H...O and C—H...O hydrogen bonds and iodo...nitro and aromatic π...π stacking interactions. Comparisons are made between the supramolecular structures of these compounds and those of other isomers, in terms both of the types of direction-specific intermolecular interactions exhibited and the dimensionality of the resulting supramolecular structures.
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Agbo, Gildenhuys та Mphahlele. "Inhibitory Effects of Novel 7-Substituted 6-iodo-3-O-Flavonol Glycosides against Cholinesterases and β-secretase Activities, and Evaluation for Potential Antioxidant Properties". Molecules 24, № 19 (2019): 3500. http://dx.doi.org/10.3390/molecules24193500.

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A series of 7-halogeno- (X = F, Cl, Br) and 7-methoxy-substituted acetylated 6-iodo-3-O-flavonol glycosides were prepared, and evaluated for inhibitory effect in vitro against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) activities. 7-Bromo-2-(4-chlorophenyl)-6-iodo-4H-chromen-4-one-3-O-2,3,4,6-O-tetraacetyl-β-d-glucopyranoside (2k) and 7-bromo-6-iodo-2-(4-methoxyphenyl)-4H-chromen-4-one-3-O-2,3,4,6-O-tetraacetyl-β-d-glucopyranoside (2l) exhibited significant inhibitory effect against AChE activity when compared to the activity of the reference standard, donepezil. Compound 2k was found to be selective against AChE and to exhibit reduced inhibitory effect against BChE activity. 6-Iodo-7-methoxy-2-(4-methoxyphenyl)-4H-chromen-4-one-3-O-2,3,4,6-O-tetraacetyl-β-d-glucopyranoside (2p) was found to exhibit increased activity against BChE, more so than the activity of donepezil. The most active compounds were also evaluated for inhibitory effect against β-secretase activity and for potential radical scavenging activities. The experimental data were complemented with molecular docking (in silico) studies of the most active compounds into the active sites of these enzymes.
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Dissertations / Theses on the topic "Iodo-compounds"

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Carvalho, Paulo Sergio de 1966. "Ciclizações oxidativas de 3-hidróxi-benzenopropanóis promovidas por reagentes de iodo(III) hipervalente." [s.n.], 2013. http://repositorio.unicamp.br/jspui/handle/REPOSIP/250616.

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Orientador: Jose Augusto Rosário Rodrigues<br>Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Química<br>Made available in DSpace on 2018-08-24T08:17:01Z (GMT). No. of bitstreams: 1 Carvalho_PauloSergiode_D.pdf: 14146737 bytes, checksum: cce704fa63bb067ebc25618dac57ceb6 (MD5) Previous issue date: 2013<br>Resumo: Este trabalho descreve uma metodologia para a síntese de 1,2- e 1,4-benzoquinona-monocetais através da oxidação de fenóis contendo uma cadeia hidróxi-alquílica lateral promovida por reagentes de iodo(III) hipervalente. 3-Hidróxi-?-metil-benzenopropanol e três derivados metoxilados foram preparados a partir dos respectivos benzaldeídos. Oxidações do 3-hidróxi-?-metil-benzenopropanol com um equivalente de diacetato de iodobenzeno (IBDA) ou [bis(trifluoroacetóxi)iodobenzeno] (BTIB) em diversos solventes não renderam o croman-6-ol esperado, mas apenas materiais poliméricos marrons. Entretanto, resultados interessantes foram obtidos das oxidações dos benzenopropanóis com dois equivalentes de IBDA em metanol ou 2,2,2-trifluoroetanol (TFE). Em metanol, 4,4-dimetóxi-cicloexa-2,5-dienonas e 6,6-dimetóxi-cicloexa-2,4-dienonas foram os produtos principais, enquanto que, em TFE, ciclizações da cadeia hidróxi-alquílica lateral não-rígida originaram monocetais semicíclicos de 1,2- e 1,4-benzoquinonas como produtos principais. A oxidação do 3-hidróxi-?-metil-4-metóxi-benzenopropanol em metanol rendeu um dímero de Diels-Alder mediante a cicloadição da respectiva cicloexa-2,4-dienona. As sínteses desses monocetais semicíclicos são importantes por se tratarem dos primeiros exemplos de cetais derivados de cromanóis obtidos por oxidações de fenóis contendo uma cadeia lateral não-rígida. A parte final do trabalho descreve as primeiras etapas de uma síntese do (S)-6-benzilóxi-2,5,7,8-tetrametil-croman-2-carbaldeído, proposta com base na metodologia desenvolvida. A síntese desse heterociclo representaria uma nova síntese formal da vitamina E (?-tocoferol).<br>Abstract: A methodology to the synthesis of 1,2- and 1,4-benzoquinone semicyclic monoketals through the oxidation of phenols bearing a hydroxy-alkyl side chain promoted by hypervalent iodine(III) reagents is described. 3-Hydroxy-?-methyl-benzenepropanol and three of its methoxy derivatives were prepared from the respective benzaldehydes. Oxidations of 3-hydroxy-?-methyl-benzenepropanol with one equivalent of iodobenzene diacetate (IBDA) or [bis(trifluoroacetoxy)iodobenzene] (BTIB) in a variety of solvents did not furnish the expected chroman-6-ol; instead, only red-brownish polymeric materials were produced. However, better results were achieved from the oxidations of the benzenepropanols by two equivalents of IBDA in methanol or 2,2,2-trifluoroethanol (TFE) as solvent. In methanol, 4,4-dimethoxy-cyclohexa-2,5-dienones and 6,6-dimethoxy-cyclohexa-2,4-dienones were the major products, whereas in TFE, cyclizations of the nonrigid hydroxy-alkyl side chain took place to furnish 1,2- and 1,4-benzoquinone semicyclic monoketals as main products. The oxidation of the 3-hydroxy-4-methoxy derivative in methanol yielded only a Diels-Alder dimer by the cycloaddition of the unstable intermediate cyclohexa-2,4-dienone. The syntheses of the semicyclic monoketals described here represent an important achievement since these are the first examples of semicyclic ketals related to chromanols obtained by the oxidation of phenols having a nonrigid hydroxy-alkyl side chain. The final part of this work describes the initial efforts towards the synthesis of (S)-6-benzyloxy-2,5,7,8-tetramethyl-chroman-2-carbaldehyde, proposed on the basis of the developed methodology. The synthesis of this heterocyclic compound would represent a new formal synthesis of vitamin E (?-tocopherol).<br>Doutorado<br>Quimica Organica<br>Doutor em Ciências
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Tanaka, Hisaaki, Hideshi Nishiyama, Shin-ichi Kuroda, Takami Yamashita, Minoru Mitsumi, and Koshiro Toriumi. "ESR observation of optically generated solitons in the quasi-one-dimensional iodo-bridged diplatinum complex Pt_2(n-pentylCS_2)_4I." American Physical Society, 2008. http://hdl.handle.net/2237/11299.

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MOURA, JOAO A. "Desenvolvimento e construção de sistema automatizados para controle de qualidade na produção de sementes de iodo-125." reponame:Repositório Institucional do IPEN, 2015. http://repositorio.ipen.br:8080/xmlui/handle/123456789/26454.

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Submitted by Claudinei Pracidelli (cpracide@ipen.br) on 2016-07-01T11:08:37Z No. of bitstreams: 0<br>Made available in DSpace on 2016-07-01T11:08:37Z (GMT). No. of bitstreams: 0<br>Tese (Doutorado em Tecnologia Nuclear)<br>IPEN/T<br>Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP
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Malan, Christophe. "Synthèse de dérivés bores pour la boroneutrothérapie." Université Joseph Fourier (Grenoble), 1997. http://www.theses.fr/1997GRE10124.

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Dans ce travail, la synthese d'acides alpha-amines bores tels que la borophenylalanine-compose actuellement en essais cliniques chez l'homme pour le traitement des melanomes par boroneutrotherapie- et divers de ses analogues a ete abordee. Diverses approches d'une synthese stereospecifique de la l-borophenylalanine (ce qui n'avait jamais ete realise auparavant), ont ete envisagees. La premiere, dont l'etape clef repose sur une reaction de couplage entre un organozincique chiral derive de la l-serine et un iodure aromatique bore, a permis d'obtenir la l-borophenylalanine optiquement pure. La deuxieme voie d'acces a fait appel a une transamination enzymatique de l'acide 4-boronophenylpyruvique. Les resultats preliminaires de la reaction enzymatique (effectuee a l'universite de clermont-ferrand) montrent que la borophenylalanine est effectivement produite. Des etudes complementaires concernant cette reaction sont actuellement menees. Une troisieme voie d'acces a la l-borophenylalanine a mis en jeu un couplage catalyse au palladium (0) entre un diboronate et des derives de la l-iodophenylalanine, ce qui en a fait la synthese la plus courte et la plus performante. Par ailleurs, la preparation d'analogues bores de la dopa a ete abordee, ce qui a conduit a preparer des dehydroaminoesters aromatiques bores dont la reduction n'a malheureusement pu etre effectuee. La preparation d'acides amines carboranes, analogues de la borophenylalanine, a constitue un autre axe de recherches et a demande la mise au point d'une monofonctionnalisation performante du para-carborane, ce qui a permis l'acces a deux nouvelles classes des para-carboranes : les para-carboranols et les acides para-carboranylboroniques. Enfin, un groupement protecteur de la fonction acide boronique d'un type nouveau, permettant le deblocage dans des conditons reductrices douces, a ete developpe et son utilisation s'est revelee determinante a plusieurs occasions au cours de ce travail.
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Conan, Françoise. "Contribution à l'élaboration de nouveaux squelettes organiques via l'étude de la réactivité d'un groupe disulfure de carbone coordine au molybdène." Brest, 1988. http://www.theses.fr/1988BRES2017.

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La reactivite du complexe du titre est etudiee vis a vis d'alcynes portant des groupes electroattracteurs. On obtient des complexes metallocycliques a liaison molybdene-carbone ou molybdene-soufre. On prepare un complexe original par addition de trois molecules de propiolonitrile. On etudie egalement la reactivite de ces composes heterocycliques vis a vis de ch::(3)i, nabh::(4) et de hc=c-cn
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Estel, Lionel. "Fonctionnalisation d'aminopyridines par métallation : application à la synthèse d'hétérocycles." Rouen, 1988. http://www.theses.fr/1988ROUES035.

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L'action d'aldéhydes aromatiques sur des pivalolaminopyridines ortho lithiées a donné des alcools secondaires qui ont été oxydés en cétones. Ceci permettant une synthèse en 4 étapes des amino-2 pyridyl-3, amino-3 pyridyl-4 et amino-4 pyridyl-3 arylméthanones. De la même façon, la fluoro-4 lithio-3 pyridine conduit à l'amino-4 pyridyl-3 phénylméthanone. Pour montrer l'intérêt de la méthode, des pyridopyrimidinones et des benzonaphtyridines ont été synthétisées. Par ailleurs, la fluoro-2 pyridine métallée, réagit avec l'iode pour donner des iodo-3 pyridines diversement substituées en 2. Une synthèse en 2 étapes des ortho iodo aminopyridines a été développée à partir des trois monoaminopyridines. La substitution de l'iode par des énolates dans les conditions de la SNR1 conduit après cyclisation acide aux aza-5, -6 et -7 indoles substitués en 2. Enfin, des aza-5 indoles disubstitués en -2, -3 ont été obtenus par action d'alphaméthoxycétones sur la lithio-3 pivalamido-4 pyridine et cyclisation acide
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Lesenyeho, Lehlogonolo Godfrey. "Palladium-catalyzed heteroannulation of 2-ARYL- 3-IODO-4-(Phenylamino)quinolines and 4-(N,N-allylphenylamino)-2-ARYL-3-iodoquinolines." Diss., 2010. http://hdl.handle.net/10500/3970.

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The previously described 2-aryl-4-chloro-3-iodoquinolines were prepared following literature procedure and in turn converted to the corresponding hitherto unknown 2-aryl-3-iodo-4-(phenylamino)quinoline derivatives using aniline in refluxing ethanol. These 2-aryl-3-iodo-4-(phenylamino)quinolines were reacted with allybromide in ethanol at room temperature to afford 4-(N,N-allylphenylamino)-2-aryl-3-iodoquinoline derivatives. The 2-aryl-3-iodo-4-(phenylamino)quinoline and 4-(N,N-allylphenylamino)-2-aryl-3-iodoquinoline derivatives were subjected to metal-catalysed carbon-carbon bond formations. Palladium(0)-copper iodide catalysed Sonogashira cross-coupling of 2-aryl-3-iodo-4-(phenylamino)quinoline with terminal alkynes afforded series of 1,2,4-trisubstituted 1H-pyrrolo[3,2-c]quinolines in a single step operation. On the other hand, the 4-(N,N-allylphenylamino)-2-aryl-3-iodoquinoline derivatives were found to undergo palladium-catalysed intramolecular Heck reaction to yield the corresponding 1,3,4-trisubstituted 1H-pyrrolo[3,2-c]quinolines. All new compounds were characterized by using a combination of NMR (1H and 13C), IR, mass spectroscopic techniques as well as elemental analysis.<br>Chemistry<br>MSc. (Chemistry)
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Book chapters on the topic "Iodo-compounds"

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Dohi, Toshifumi, and Yasuyuki Kita. "Reaction of Iodo Compounds." In Iodine Chemistry and Applications. John Wiley & Sons, Inc, 2014. http://dx.doi.org/10.1002/9781118909911.ch17.

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Burton, Donald J., and Ling Xue. "Preparation of (Z)-2-iodo-1,2-Difluorostyrenes." In Efficient Preparations of Fluorine Compounds. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118409466.ch37.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iodo bridged niobium complex of mesitylene." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_158.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of heterobimetallic cobalt-molybdenum, sulfido-iodo cluster." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_299.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(II) iodo complex with polythioether ligand." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_69.

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Burton, Donald J., and Craig A. Wesolowski. "Preparation of 1,4-Bis(Z-2-iodo-1,2-difluoroethenyl)benzene." In Efficient Preparations of Fluorine Compounds. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118409466.ch38.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) iodo complex with neutral malonamide." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_754.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) iodo complex with triethyl-phosphine oxide." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_360.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) iodo complex with tripropyl-phosphine oxide." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_363.

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10

Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) iodo complex with tributyl-phosphine oxide." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_365.

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Conference papers on the topic "Iodo-compounds"

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Kepeňová, Martina, Michaela Benediková, Mária Vilková, Miroslava Litecká, and Ivan Potočňák. "Ionic palladium(II) complexes with nitro and halogen derivatives of 8-hydroxyquinoline." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.443k.

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Abstract:
Four commercially unavailable derivatives of 8-hydroxyquinoline with different functional groups (nitro and halogen) in positions 5 and 7 were prepared: 5-nitro-7-iodo-8-hydroxyquinoline (HNIQ), 5-nitro-7-bromo-8-hydroxyquinoline (HNBrQ), 5-iodo-7-bromo-8-hydroxyquinoline (HIBrQ) and 5-chloro-7-bromo-8-hydroxyquinoline (HClBrQ). Their characterization was performed by IR and NMR spectroscopy, elemental analysis and in the case of HIBrQ and HClBrQ by single crystal X-ray structure analysis. Prepared compounds were used for the synthesis of new palladium(II) complexes NH2(CH3)2[PdCl2(XQ)], where XQ = NIQ (1), NBrQ (2), IBrQ (3) and ClBrQ (4). IR and NMR spectroscopy, elemental and X-ray structure analysis were used for their characterization. Bidentate chelate coordination of one molecule of XQ through nitrogen and oxygen atoms in square planar complexes was found. These complexes represent a group of compounds in which biological activities were found and will be used for the following biological study.
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