Gotowe bibliografie tematyczne / Imines

Gotowa bibliografia na temat „Imines”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 28 lipca 2024

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Artykuły w czasopismach na temat "Imines"

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Svete, Jurij, Uroš Grošelj, Franc Požgan i Bogdan Štefane. "Copper-Catalyzed Azomethine Imine–Alkyne Cycloadditions (CuAIAC)". Synthesis 50, nr 23 (5.10.2018): 4501–24. http://dx.doi.org/10.1055/s-0037-1610284.

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Although the first example of copper-catalyzed azomethine imine–alkyne cycloaddition (CuAIAC) was published only a year after the seminal papers of Meldal and Sharpless on Cu-catalyzed azide–alkyne cycloaddition (CuAAC), the CuAIAC reaction has remained overlooked by the synthetic community for almost a decade. Since 2010, however, CuAIAC reaction started to emerge as a promising supplement to the well-known CuAAC reaction. The present review surveys primarily the literature on CuAIAC reaction since 2003. Beside this, azomethine imine–alkyne cycloadditions catalyzed by other metals, selected examples of metal-free reactions, and related [3+3] and [3+4] cycloadditions of azomethine imines are presented. All these experimental data indicate the viability of CuAIAC in organic synthesis and the applicability in ‘click’ chemistry.1 Introduction2 Reactions with Acyclic Azomethine Imines3 Reactions with C,N-Cyclic Azomethine Imines4 Reactions with N,N-Cyclic Azomethine Imines5 Reactions with C,N,N-Cyclic Azomethine Imines6 The Mechanism of the CuAIAC Reaction7 Conclusions and Outlook
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Wulff, William, Xin Zhang i Yijing Dai. "The Acceleration of the Rearrangement of α-Hydroxy Aldimines by Lewis or Brønsted Acids". Synlett 29, nr 15 (28.08.2018): 2015–18. http://dx.doi.org/10.1055/s-0037-1610262.

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An efficient method was developed for the synthesis of α-amino ketones from α-hydroxy imines. The reaction occurs through an α-iminol rearrangement involving the migration of a substituent of the carbinol carbon to the imine carbon. The optimal catalysts were found to be silica gel or montmorillonite K 10, which effected migration of a variety of aryl and alkyl substituents in high yields. The rearrangement can also be carried out on imines generated in situ from aldehydes and amines in essentially the same yields as those from the preformed imines.
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Gonciarz, Agnieszka, Robert Pich, Krzysztof Artur Bogdanowicz, Beata Jewloszewicz, Wojciech Przybył, Karolina Dysz, Agnieszka Dylong i in. "UV–Vis Absorption Properties of New Aromatic Imines and Their Compositions with Poly({4,8-bis[(2-Ethylhexyl)oxy]Benzo[1,2-b:4,5-b′]Dithiophene-2,6-diyl}{3-Fluoro-2-[(2-Ethylhexyl)Carbonyl]Thieno[3,4-b]Thiophenediyl})". Materials 12, nr 24 (13.12.2019): 4191. http://dx.doi.org/10.3390/ma12244191.

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In this paper, four new aromatic imines containing at least one thiazole-based heterocycle were analyzed in detail by UV–Vis spectroscopy, taking into consideration their chemical structures and interactions with PTB7, a known polymeric electron donor widely used in bulk heterojunction organic solar cells. It is demonstrated that the absorption spectra of the investigated active compositions can be modified not only by changing the chemical structure of imine, but also via formulations with PTB7. For all investigated imines and PTB7:imine compositions, calibration curves were obtained in order to find the optimum concentration in the composition with PTB7 for expansion and optimization of absorption spectra. All imines and PTB7:imine compositions were investigated in 1,2-dichlorobenzene by UV–Vis spectroscopy in various concentrations, monitoring the changes in the π–π* and n–π* transitions. With increasing imine concentrations, we did not observe changes in absorption maxima, while with increasing imine concentrations, a hypochromic effect was observed. Finally, we could conclude that all investigated compositions exhibited wide absorptions of up to 800 nm and isosbestic points in the range of 440–540 nm, confirming changes in the macromolecular organization of the tested compounds. The theoretical calculations of their vibration spectra (FTIR) and LUMO–HOMO levels by Density Functional Theory (DFT) methods are also provided. Finally, IR thermal images were measured for organic devices based on imines and the imine:PTB7 composite.
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Mendes, Joseane A., Paulo R. R. Costa, Miguel Yus, Francisco Foubelo i Camilla D. Buarque. "N-tert-Butanesulfinyl imines in the asymmetric synthesis of nitrogen-containing heterocycles". Beilstein Journal of Organic Chemistry 17 (12.05.2021): 1096–140. http://dx.doi.org/10.3762/bjoc.17.86.

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The synthesis of nitrogen-containing heterocycles, including natural alkaloids and other compounds presenting different types of biological activities have proved to be successful employing chiral sulfinyl imines derived from tert-butanesulfinamide. These imines are versatile chiral auxiliaries and have been extensively used as eletrophiles in a wide range of reactions. The electron-withdrawing sulfinyl group facilitates the nucleophilic addition of organometallic compounds to the iminic carbon with high diastereoisomeric excess and the free amines obtained after an easy removal of the tert-butanesulfinyl group can be transformed into enantioenriched nitrogen-containing heterocycles. The goal of this review is to the highlight enantioselective syntheses of heterocycles involving the use of chiral N-tert-butanesulfinyl imines as reaction intermediates, including the synthesis of several natural products. The synthesis of nitrogen-containing heterocycles in which the nitrogen atom is not provided by the chiral imine will not be considered in this review. The sections are organized according to the size of the heterocycles. The present work will comprehensively cover the most pertinent contributions to this research area from 2012 to 2020. We regret in advance that some contributions are excluded in order to maintain a concise format.
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Garrido-Castro, Alberto F., M. Carmen Maestro i José Alemán. "α-Functionalization of Imines via Visible Light Photoredox Catalysis". Catalysts 10, nr 5 (19.05.2020): 562. http://dx.doi.org/10.3390/catal10050562.

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The innate electrophilicity of imine building blocks has been exploited in organic synthetic chemistry for decades. Inspired by the resurgence in photocatalysis, imine reactivity has now been redesigned through the generation of unconventional and versatile radical intermediates under mild reaction conditions. While novel photocatalytic approaches have broadened the range and applicability of conventional radical additions to imine acceptors, the possibility to use these imines as latent nucleophiles via single-electron reduction has also been uncovered. Thus, multiple research programs have converged on this issue, delivering creative and practical strategies to achieve racemic and asymmetric α-functionalizations of imines under visible light photoredox catalysis.
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Nugent, Thomas C., Richard Vaughan Williams, Andrei Dragan, Alejandro Alvarado Méndez i Andrei V. Iosub. "An investigation of the observed, but counter-intuitive, stereoselectivity noted during chiral amine synthesis via N-chiral-ketimines". Beilstein Journal of Organic Chemistry 9 (15.10.2013): 2103–12. http://dx.doi.org/10.3762/bjoc.9.247.

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The default explanation for good to high diastereomeric excess when reducing N-chiral imines possessing only mediocre cis/trans-imine ratios (>15% cis-imine) has invariably been in situ cis-to-trans isomerization before reduction; but until now no study unequivocally supported this conclusion. The present study co-examines an alternative hypothesis, namely that some classes of cis-imines may hold conformations that erode the inherent facial bias of the chiral auxiliary, providing more of the trans-imine reduction product than would otherwise be expected. The ensuing experimental and computational (DFT) results favor the former, pre-existing, explanation.
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Rawaa Daoud Sulaiman i Zaheda Ahmed Najim. "The Effect of Temperature and Thermodynamic Parameters on the Ionization Constants of Some Imines Derived from Vanillin with substituted aniline". Tikrit Journal of Pure Science 27, nr 4 (28.11.2022): 31–38. http://dx.doi.org/10.25130/tjps.v27i4.30.

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This work presents a method for the preparation of imine compounds including Schiff bases derived from vanillin with aniline, o-nitroaniline, o-tolidene and o-chloroaniline. Compounds' structures of the prepared compounds were confirmed by physical methods like melting point, infrared spectroscopy (IR), electronic spectroscopy (U.V), and nuclear magnetic resonance spectroscopy (NMR). The ionization constants of the imine nitrogen proton Ka1 and the phenol hydroxyl group proton Ka2 were determined using the spectrometric titration method at five temperatures including 293,298,303,308 and 313K in a buffer solution medium. The thermodynamic of ionization for imines confirm that ionization reactions in these imines are accompanied by an increase of parameters ∆Gº and ∆Hº. These mean that ionization reactions in these imines are non-spontaneous and endothermic respectively. ∆Sº values of ionization reactions estimated have a negative and a positive signs.
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An, Ran, Mengbi Guo, Yingbo Zang, Hang Xu, Zhuang Hou i Chun Guo. "Recent Advances in Synthesis of Benzazoles via Imines". Current Organic Chemistry 24, nr 17 (12.11.2020): 1897–942. http://dx.doi.org/10.2174/1385272824999200818180845.

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Imines, versatile intermediates for organic synthesis, can be exploited for the preparation of diverse classes of biologically active benzazoles. Because of the special characteristics of the C=N bond, imines can be simultaneously used in the synthesis of 1,3-benzazoles and 1,2-benzazoles. With the development of imine synthesis, a variety of novel cascade reactions for benzazole synthesis have been reported in the last decade. Therefore, there is a strong need to elucidate the recent progress in the formation of various classes of benzazoles, including benzimidazoles, benzoxazoles, benzothiazoles, indazoles, and benzisoxazoles, via imines obtained by condensation reactions or oxidative/ redox coupling reactions
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Freese, Tyll, Jan C. Namyslo, Martin Nieger i Andreas Schmidt. "Sulfur, mercury, and boron adducts of sydnone imine derived anionic N-heterocyclic carbenes". RSC Advances 9, nr 9 (2019): 4781–88. http://dx.doi.org/10.1039/c9ra00294d.

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The sydnone imines (5-benzoylimino)-3-(2-methoxyphenyl)-sydnone imine and molsidomine were deprotonated at C4 to give sydnone imine anions which can be represented as anionic N-heterocyclic carbenes, respectively.
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Zhang, Hanmo, E. Ben Hay, Stephen J. Geib i Dennis P. Curran. "Fates of imine intermediates in radical cyclizations of N-sulfonylindoles and ene-sulfonamides". Beilstein Journal of Organic Chemistry 11 (17.09.2015): 1649–55. http://dx.doi.org/10.3762/bjoc.11.181.

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Two new fates of imine intermediates formed on radical cyclizations of ene-sulfonamides have been identified, reduction and hydration/fragmentation. Tin hydride-mediated cyclizations of 2-halo-N-(3-methyl-N-sulfonylindole)anilines provide spiro[indoline-3,3'-indolones] or spiro-3,3'-biindolines (derived from imine reduction), depending on the indole C2 substituent. Cyclizations of 2-haloanilide derivatives of 3-carboxy-N-sulfonyl-2,3-dihydropyrroles also presumably form spiro-imines as primary products. However, the lactam carbonyl group facilitates the ring-opening of these cyclic imines by a new pathway of hydration and retro-Claisen-type reaction, providing rearranged 2-(2'-formamidoethyl)oxindoles.
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Rozprawy doktorskie na temat "Imines"

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Lavergne, Kaitlyn. "Synthesis of Azomethine Imines via Alkene Aminocarbonylation and their Derivatization into Pyrazolones". Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/32516.

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Nitrogen-containing heterocyclic compounds are very important to the pharmaceutical and agrochemical industries, among others. Over the past few years, the Beauchemin group has been exploring reactivity of N-substituted isocyanates and as part of this has developed a metal-free alkene aminocarbonylation process relying on imino-isocyanates to form azomethine imines. The azomethine imines formed are interesting since they contain a cyclic β-aminocarbonyl motif. Catalysis of this reaction using basic additives allowed milder reaction conditions with electron-rich C=C bonds such as enol ethers. Efforts have also been made towards the derivatization of these azomethine imines into useful products. It was discovered that upon reduction and aromatization of azomethine imines, pyrazolones could be obtained. This is providing a novel modular approach to these compounds, which have relevance in pharmaceuticals and agrochemicals. This reactivity was extended to include imino-isothiocyanates.
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Young, Adrian R. "Free radical cyclisation of imines". Thesis, Loughborough University, 1996. https://dspace.lboro.ac.uk/2134/15357.

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Introduction. The free radical cyclisation reaction onto an unsaturated bond is a well known synthetic pathway, where a wide range of cyclic compounds can be produced form acyclic starting materials. Up until recent years, free radical addition to multiple bonds other than carbon-carbon had been little studied. Nowadays there is much information available of radical addition to carbonyl, thiocarbonyl, nitrile and oxime ether (C=NOR) functional groups. However there has been surprisingly little detailed study of similar reactions involving imines (C=NR) or hydrazones (C=NNHR). Monocyclisation. In the early phase of the research, different types of imine were synthesised and subjected to the standard free radical cyclisation procedure (tributyl-tin hydride / AIBN, added by syringe pump to refluxing solvent) to determination of the regiochemistry of cyclisation onto imines and to assess the synthetic potential of the reaction. The results of this investigative study show that a variety of five and six-membered ring compounds can be synthesised in good yield. A similar study of hydrazones showed that fivemembered rings can be formed under the same reaction conditions. Tandem Reactions. In the next phase, the aim was to extend the methodology to produce more complex structures from acyclic starting materials. If a radical adds to the carbon atom of an imine, a nitrogen-centred (aminyl) radical is generated which can undergo subsequent addition to a suitably positioned double bond to yield a bicyclic amine. This type of reaction is known as tandem or cascade cyclisation. By this method, compounds could be synthesised which have similar structures to natural products. A range of suitably designed imines wct.5. prepared and underwent cyclisation, producing many different types of bicyclic amine in yields varying from moderate to good. The Synthesis of Natural Products. After the successful formation of key bicyclic structures, the third phase of the research aimed at the synthesis of one or more of target natural products. The synthetic strategy used in the tandem reactions outline above was. adapted for these purposes. However the synthesis of the desired compounds could not be achieved in the time, but progress towards their formation was achieved.
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Tillman, Anna Louise. "Organocatalytic, enantioselective additions to imines". Thesis, University of Cambridge, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612994.

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Heaney, Mary Frances Teresa. "Cycloaddition reactions of oximes and imines". Thesis, Queen's University Belfast, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.335415.

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Black, Daniel. "Imines in copper-catalyzed cross-coupling reactions". Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=102960.

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The purpose of this study was to develop new catalytic methods to mediate carbon-carbon bond forming reactions with imines under mild conditions and in a general manner. We found that copper catalysts were compatible in cross-coupling of a range of mild organometallic reagents, providing simple, efficient routes to alpha-substituted amides and amines.
Chapter 2 of this thesis describes a new copper-catalyzed multicomponent synthesis of alpha-substituted amides. This reaction was developed based upon previous work in this laboratory, which showed that palladium catalysts were competent in Stille-type cross-coupling of imines, acid chlorides, and organostannanes. While providing a mild method of generating the amide products, a more general procedure able to incorporate a wider range of organostannanes was sought. This chapter details the development of a copper-catalyzed protocol, which, as well as performing the cross-coupling under mild reaction conditions, proceeds with a diverse range of aryl-, heteroaryl-, and vinyl-substituted organostannanes and employs an inexpensive and readily available catalyst. Through this system, control over regioselectivity of addition to alpha,beta-unsaturated imines is also possible.
Chapter 3 demonstrates that, in addition to organostannanes, other substrates are viable in copper-catalyzed cross-coupling with imines and acid chlorides. Herein, the coupling of terminal alkynes with imines and acid chlorides is described, leading to an efficient synthesis of tertiary propargylamides directly from simple starting materials. This synthesis incorporates a wide variety of substituted imines, acid chlorides/chloroformates, and terminal alkynes, providing a rapid synthesis of these useful building blocks (reaction completion in only 15 minutes). In addition, the process is shown to work with aza-aromatic heterocycles, such as pyridine, where the alkynylation occurs exclusively at the 2-position.
Chapter 4 describes the utility of these rapid multicomponent reactions, where the products are directly converted into oxazole heterocycles. Copper-catalyzed- and zinc-catalyzed protocols are developed for the synthesis of secondary propargylamides from silyl-imines, acid chlorides, and terminal alkynes. The secondary propargylamide products are then, in a one pot sequence, transformed into trisubstituted oxazoles.
Chapter 5 describes the development of an atom-economical, non-toxic alternative to the organotin coupling described in Chapter 2. This involves the use of tri- and tetraorgano-indium reagents, which can transfer all of their organic groups in a copper-catalyzed coupling with imines and acid chlorides. This reaction shows good functional group compatibility and further expands the scope of alpha-substituted amides and N-protected amines that can be synthesized through mild copper catalysis.
Chapter 6 explores the enantioselective alkynylation of nitrogen-containing heterocycles. As described in Chapter 3, heterocycles such as pyridine can undergo copper-catalyzed 1,2-addition with terminal alkynes upon activation by chloroformates. As this process generates a stereocenter, it is possible to introduce enantio-control into the reactions by using a chiral copper catalyst. With ligands from the PINAP series, enantioselectivities of up to 84% can be induced in the coupling of nitrogen-containing heterocycles (e.g., quinoline), chloroformates, and terminal alkynes. This provides a mild and simple synthesis of chiral 2-alkynyl-1,2-dihydroquinolines directly from simple starting materials.
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Kovaricek, Petr. "Motional, reactional and constitutional dynamics of imines". Phd thesis, Université de Strasbourg, 2014. http://tel.archives-ouvertes.fr/tel-01059611.

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Les travaux réalisées lors de cette thèse s'intéressent aux dynamiques de mouvement, de réaction et de constitution des fonctions imines. Les aldéhydes les plus réactives pour cette réaction de condensation ont été identifiées. Un processus d'échange intramoléculaire aléatoire rapide a été observé entre le salicylaldéhyde et l'éthylènediamine dont la vitesse est contrôlée par les substituants, la longueur de la chaîne amine, le solvant et la température. Cette observation conduità l'élaboration de mouvements de déplacement d'abord non-directionnels puis développés pour devenir directionnels. Une sélectivité dynamique réactionnelle a été introduite sur des mélanges d'aldéhydes et d'amines. Elle a été baptisée simpléxité et est utilisée pour de la protection de fonctions. Enfin, la nature dynamique de l'imine a été étudiée à l'interface solide-liquide parmicroscopie à effet tunnel et montre une accélération et une amplification des produits formées sur la surface.
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Hartley, James Holroyd. "Saccharide accelerated hydrolysis of boronic acid imines". Thesis, University of Birmingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.369335.

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Rajamäki, Suvi Henna Maria. "Lewis acid mediated cyclisations of methylenecyclopropyl imines". Thesis, University of Southampton, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.401829.

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Guillemin, Jean-Claude. "Les imines non-stabilisees : synthese et reactivite". Rennes 1, 1986. http://www.theses.fr/1986REN10053.

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Guillemin, Jean-Claude. "Les Imines non-stabilisées synthèse et réactivité". Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb37598084v.

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Książki na temat "Imines"

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Johnson, A. William. Ylides and imines of phosphorus. New York: Wiley, 1993.

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Kimpe, Norbert De. The chemistry of &-haloketones, &-haloaldehydes and &-haloimines. Chichester, England: Wiley, 1988.

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Hartley, James Holroyd. Saccharide accelerated hydrolysis of boronic acid imines. Birmingham: University of Birmingham, 2000.

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Kimpe, Norbert de. The chemistry of [alpha]-haloketones, [alpha]-haloaldehydes, and [alpha]-haloimines. Chichester: Wiley, 1988.

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Hallett, David James. Ally lstannanes: Reaction with imines, iminium ions and ketones. Manchester: University of Manchester, 1993.

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Rahid, H. S. New syntheses of imines and chiral B-aminophosphine derivatives. Manchester: UMIST, 1997.

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Power, Nicholas Patrick. Kinetics and mechanisms of reactions of N-Arylsulfonyl derivatives of imines. [S.l: The Author], 1998.

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Center, Langley Research, red. Modified phenylethynyl containing imides for secondary bonding: Non-autoclave, low twmperature processable adhesives. Hampton, Va: National Aeronautics and Space Administration, Langley Research Center, 1999.

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Mazurkiewicz, Roman. Studium reakcji imidoilowania amidów. Gliwice: Politechnika Śląska, 1989.

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Center, Langley Research, i United States. National Aeronautics and Space Administration., red. Synthesis and characterization of modified phenylethynyl terminated polyimides. Hampton, Va: National Aeronautics and Space Administration, Langley Research Center, 1998.

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Części książek na temat "Imines"

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Rowlands, C. C., i R. D. Farley. "15.7.2 Imines and imides". W Landolt-Börnstein - Group II Molecules and Radicals, 446–54. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-45824-1_56.

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Dilworth, J. R., i S. Morton. "From Imines". W Inorganic Reactions and Methods, 41–43. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145227.ch25.

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Ojima, I. "Of Imines". W Inorganic Reactions and Methods, 255–57. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145319.ch83.

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Li, Wei, i Xumu Zhang. "Asymmetric Hydrogenation of Imines". W Stereoselective Formation of Amines, 103–44. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/128_2013_483.

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Martin, Dean F., i Edward J. Olszewski. "Metal Derivatives of β-Keto Imines (β-Imino Ketones)". W Inorganic Syntheses, 45–52. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132395.ch14.

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Sharp, John T. "Nitrile Ylides and Nitrile Imines". W Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products, 473–537. New York, USA: John Wiley & Sons, Inc., 2003. http://dx.doi.org/10.1002/0471221902.ch7.

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Vilariño, Natalia, Sara F. Ferreiro, Andrés Crespo i José Gil. "Pharmacology of the cyclic imines". W Phycotoxins, 343–60. Chichester, UK: John Wiley & Sons, Ltd, 2015. http://dx.doi.org/10.1002/9781118500354.ch15.

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Bailey, Patrick D., i Keith M. Morgan. "Enamines". W Organonitrogen Chemistry. Oxford University Press, 2022. http://dx.doi.org/10.1093/hesc/9780198557753.003.0008.

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This chapter looks into imines. It enumerates the key features of imines: oxidation level two, susceptibility to nucleophilic attack on carbon, and easy protonation in relation to producing reactive iminium ions. Imines are prepared from the reaction of an aldehyde or a ketone with a primary amine. Thus, the reaction is driven primarily through the removal of water. Imine will be more stable than simple aliphatic imines if it is conjugated by an aromatic ring. The chapter discusses the reactions of imines through attack by carbon nucleophiles, the Vilsmeyer reaction, the Mannich reaction, reduction, and hydrolysis. Additionally, the chapter shows that the reduction to amines is readily achieved via hydrogenation of hydride reducing conditions.
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Sandler, Stanley R., i Wolf Karo. "IMINES". W Sourcebook of Advanced Organic Laboratory Preparations, 234–36. Elsevier, 1992. http://dx.doi.org/10.1016/b978-0-08-092553-0.50035-2.

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Sandler, Stanley R., i Wolf Karo. "IMINES". W Organic Functional Group Preparations, 291–322. Elsevier, 1986. http://dx.doi.org/10.1016/b978-0-08-092557-8.50016-1.

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Streszczenia konferencji na temat "Imines"

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Mas-Marzá, Elena, Ramón Arcas-Martínez, Laxman Gouda i Francisco Fabregat-Santiago. "Photoelectrosynthesis of Imines". W nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.ngfm.2019.271.

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Mas-Marzá, Elena, Ramón Arcas-Martínez, Laxman Gouda i Francisco Fabregat-Santiago. "Photoelectrosynthesis of Imines". W nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.nfm.2019.271.

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Pinho e Melo, Teresa, Ana Cabral i António d'A Rocha Gonsalves. "Intramolecular Cycloaddition of Imines of Cysteine Derivatives". W The 1st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02044.

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Margulﾏs, L., J. C. Guillemin, Brett McGuire, Anthony Remijan, Olga Dorovskaya, V. Ilyushin i R. Motiyenko. "SUBMILLIMETER WAVE SPECTROSCOPY FOR ISM: IMINES WITH INTERNAL ROTATION". W 74th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2019. http://dx.doi.org/10.15278/isms.2019.tg05.

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Diz-Gil, Raquel, Sara Bermúdez-Fernández, Paula Munín-Cruz, María Pereira i José Vila. "Preparation and crystal structure of metallated 2,4,6-trimethylaniline imines". W The 24th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08322.

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Shutalev, Anatoly. "A New Approach to the Synthesis of Hydrogenated Pyrimidine-2-imines". W The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01854.

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Raposo, M. Manuela, i M. Cidália Castro. "Synthesis and Characterization of the Photophysical Properties of Novel Heterocyclic Imines". W The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a048.

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MOHSIN, Doaa Hadi, i Zahraa Hameed KAMIL. "SYNTHESIS AND CHARACTERIZATION OF SOME NEW 1,3-OXAZEPINE COMPOUNDS". W III.International Scientific Congress of Pure,Appliedand Technological Sciences. Rimar Academy, 2021. http://dx.doi.org/10.47832/minarcongress3-3.

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Streszczenie:
In this study, bis imines were synthesized by reacting aldehyde with diamine in the presence of chloroformat (55-60˚C). In moderate yield (78-82) %, and then used in the preparation of 1, 3-Oxazepine compounds by reacting with phathalic anhydridein Benzene at (80-85 ˚C). In moderate yield (83-88) %.These vehicles have been verified using(FT-IR). Key words: Characterization, Compound, Oxazepine.
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Raposo, M. Manuela, M. Cidália Castro, R. Cristina M. Ferreira i Susana P. G. Costa. "Synthesis and evaluation of heterocyclic pyrrolidene imines as optical chemosensors". W The 19th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a021.

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Naimi-Jamal, M., i E. Ali. "Efficient synthesis of imines by MCM-41-SO3H nanocatalyst". W The 14th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00399.

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Raporty organizacyjne na temat "Imines"

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Hall, Henry K., i Jr. Polymerization of Azaethylenes (Imines) and Aza-1,3-Dienes. Potential Reactive Monomers. Fort Belvoir, VA: Defense Technical Information Center, kwiecień 1988. http://dx.doi.org/10.21236/ada194717.

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Chien, James C., i B. M. Gong. Poly(aryline imides) as E-Beam Resist: Sensitivity and Resolution. Fort Belvoir, VA: Defense Technical Information Center, styczeń 1987. http://dx.doi.org/10.21236/ada201739.

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Hall, H. K., i Jr. Synthesis and Polymerization of New Imine Monomers: Azaethylenes, Azabutadienes, and Azaallenes. Fort Belvoir, VA: Defense Technical Information Center, czerwiec 1996. http://dx.doi.org/10.21236/ada314001.

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DuBois, D. A., i R. H. Neilson. Addition Reactions of a Silylated Imino(Methylene)Phosphorane. Fort Belvoir, VA: Defense Technical Information Center, styczeń 1989. http://dx.doi.org/10.21236/ada203987.

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Gilstrap, Scott E., i Aaron Yanuzo. IMITS: Information and Clinical Technologies for the Advancement of Healthcare. Fort Belvoir, VA: Defense Technical Information Center, grudzień 2008. http://dx.doi.org/10.21236/ada611064.

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Allred, Ronald E., Richard E. Jensen, Thomas A. Donnellan, Theotis Williams i Jr. Fiber Finishes for Improving Galvanic Resistance of Imide-Based Composites. Fort Belvoir, VA: Defense Technical Information Center, luty 1998. http://dx.doi.org/10.21236/ada341614.

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Archer, D. G. Thermodynamic properties of 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide. Gaithersburg, MD: National Institute of Standards and Technology, 2006. http://dx.doi.org/10.6028/nist.ir.6645.

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Loveland, Jo L., Rick Barbour, Al Krum i August C. Neitzel. Rollout and Installation of Risk Management at the IMINT Directorate, National Reconnaissance Office. Fort Belvoir, VA: Defense Technical Information Center, grudzień 1999. http://dx.doi.org/10.21236/ada375848.

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Marks, Megan. Integrated Medical Information Technology System (IMITS): Information and Clinical Technologies for the Advancement of Healthcare. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2010. http://dx.doi.org/10.21236/ada633139.

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Cooke, Garth, Nicola Maiorana, Theodore Myers, Johnnie Jernigan i Eric N. Carlson. Integrated Maintenance Information System Diagnostic Module (IMIS-DM). Version 5.0. Fort Belvoir, VA: Defense Technical Information Center, czerwiec 1991. http://dx.doi.org/10.21236/ada237244.

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