Добірка наукової літератури з теми "Imine acids"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Imine acids".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Статті в журналах з теми "Imine acids"
Zarei, Maaroof. "One-step Synthesis of β-lactams Using Cyanuric Fluoride". Journal of Chemical Research 37, № 1 (січень 2013): 25–27. http://dx.doi.org/10.3184/174751912x13545429290478.
Повний текст джерелаWulff, William, Xin Zhang та Yijing Dai. "The Acceleration of the Rearrangement of α-Hydroxy Aldimines by Lewis or Brønsted Acids". Synlett 29, № 15 (28 серпня 2018): 2015–18. http://dx.doi.org/10.1055/s-0037-1610262.
Повний текст джерелаSikervar, Vikas, Ravindra Sonawane, Raghuramaiah Mandadapu, Amol Satish Dehade, Shrikant Abhiman Shete, and Mark Montgomery. "Lewis Acid Mediated [3+2] and [3+3] Annulations of an Azomethine Imine with Donor–Acceptor Cyclopropanes." Synthesis 53, no. 16 (May 10, 2021): 2865–73. http://dx.doi.org/10.1055/a-1503-8068.
Повний текст джерелаMorales Salazar, Daniel, Arvind Kumar Gupta та Andreas Orthaber. "Reactivity studies of an imine-functionalised phosphaalkene; unusual electrostatic and supramolecular stabilisation of a σ2λ3-phosphorus motif via hydrogen bonding". Dalton Transactions 47, № 31 (2018): 10404–9. http://dx.doi.org/10.1039/c8dt01607k.
Повний текст джерелаAlex, S., P. Turcotte, R. Fournier, and D. Vocelle. "Study of the protonation of simple Schiff bases in solvents of various polarity by means of Raman spectroscopy." Canadian Journal of Chemistry 69, no. 2 (February 1, 1991): 239–45. http://dx.doi.org/10.1139/v91-038.
Повний текст джерелаWang, Hao-Ran, En-He Huang, Chen Luo, Wen-Feng Luo, Yin Xu, Peng-Cheng Qian, Jin-Mei Zhou, and Long-Wu Ye. "Copper-catalyzed tandem cis-carbometallation/cyclization of imine-ynamides with arylboronic acids." Chemical Communications 56, no. 35 (2020): 4832–35. http://dx.doi.org/10.1039/d0cc01424a.
Повний текст джерелаBissonnette, Martine, Hoa Le Thanh, and Daniel Vocelle. "Interaction of strong acids with a conjugated imine." Canadian Journal of Chemistry 63, no. 8 (August 1, 1985): 2298–302. http://dx.doi.org/10.1139/v85-379.
Повний текст джерелаBakulina, Olga, Alexander Ivanov, Vitalii Suslonov, Dmitry Dar’in, and Mikhail Krasavin. "A speedy route to sterically encumbered, benzene-fused derivatives of privileged, naturally occurring hexahydropyrrolo[1,2-b]isoquinoline." Beilstein Journal of Organic Chemistry 13 (July 18, 2017): 1413–24. http://dx.doi.org/10.3762/bjoc.13.138.
Повний текст джерелаZaccheria, Federica, Federica Santoro, Elvina Iftitah, and Nicoletta Ravasio. "Brønsted and Lewis Solid Acid Catalysts in the Valorization of Citronellal." Catalysts 8, no. 10 (September 22, 2018): 410. http://dx.doi.org/10.3390/catal8100410.
Повний текст джерелаAhmad, Rasool, Rizwan, Altaf, Rashid, Mahmood, and Ayub. "Role of Pyridine Nitrogen in Palladium-Catalyzed Imine Hydrolysis: A Case Study of (E)-1-(3-bromothiophen-2-yl)-N-(4-methylpyridin-2-yl)methanimine." Molecules 24, no. 14 (July 17, 2019): 2609. http://dx.doi.org/10.3390/molecules24142609.
Повний текст джерелаДисертації з теми "Imine acids"
Saha, Manik Chandra. "Physico-chemical studies on coordination compounds of imine acids with dioxouranium (VI) and trivalent lanthanide ions." Thesis, University of North Bengal, 1988. http://hdl.handle.net/123456789/764.
Повний текст джерелаEvans, Caroline. "A novel methodology for the asymmetric synthesis of beta-lactams and beta-amino acids." Thesis, University of Bath, 2012. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558881.
Повний текст джерелаBaskakova, Alevtina. "Synthesis of branched [alpha]-[alpha-] and [beta]-amino[beta-amino] acids using C-nucleophile additions to imines and nitrones." Berlin Logos-Verl, 2009. http://d-nb.info/99789301X/04.
Повний текст джерелаGarbay, Guillaume. "Nouvelles voies de synthèse sans métaux d'oligomères et de polymères π-conjugués pour l'électronique organique". Thesis, Bordeaux, 2016. http://www.theses.fr/2016BORD0240/document.
Повний текст джерелаIn this work, synthesis and characterizations of new conjugated polymers are described.These polymers, developed for their integration into devices, have been synthesized via transitionmetalfree polymerizations. Carbazole based polyazomethines have been synthesized via polycondensation reactions between di-substituted carbazoles, bearing amino and formyl functionsin positions 3,6 or 2,7. Optical and electronical properties of such polymers have been studieddepending of the linkage position. A comonomer EDOT has then been integrated into the polymer chain, and impact of such insertion has been studied. Squaric and croconic acid base polymers have also been synthesized. By varying polymerization conditions, optoelectronic properties have been tuned, leading to the formation of polymers exhibiting a white emission. These polymers have then been integrated into OLED, as the active layer. Finally, more original polymers have been synthesized, using more original reactions or monomers such as by forming in situ benzobisthiazole. Other polymers integrating more originals monomers, such a tetrazine or divanillin, have been synthesized. Optoelectronic properties of such materials have been studied for the purpose of their integration into devices
Ward, Simon Edward. "Novel amino-acids from imino Diels-Alder reactions." Thesis, University of Cambridge, 1997. https://www.repository.cam.ac.uk/handle/1810/283723.
Повний текст джерелаCapra, Julien. "Synthese biomimetique de composes azotes biologiquement actifs." Thesis, Paris 11, 2011. http://www.theses.fr/2011PA112030.
Повний текст джерелаThis thesis work is devoted to the synthesis of biologically active nitrogen-containing compounds, particularly inspired by a biosynthetic reaction. Initially, our work aimed to develop a new pathway to a-amino acids using anenantioselective imine isomerization reaction. After various preliminary studies, the best precursors of a-amino acids that we have identified are a-keto amides. The 1,3isomerization of an imine formed from an a-keto amide and diphenylmethanamine using various chiral alkoxides was then conducted. The alkoxide derived from (+)-N-méthylpseudoéphédrine, employed in sub-stoichiometric quantities, allowed obtaining the corresponding a-amino amide with 67% enantiomeric excess. It still remains to develop satisfactory operating conditions for the conversion of this adduct to an a-amino acid.The study of the 1,3 isomerization of imines allowed us to bring to light a 1,4 dehydrogenation reaction, which allows an original access to 2-azadienes and which requires the presence of oxygen. Thus, several non-activated 2-azadienes have been prepared by basic treatment of imines derived from acetophenones anddiphenylmethanamine, under air atmosphere.In the last part, the study of the conjugate addition of a chiral oxazolidinone on dialkyl alkylidenemalonates was carried out, with the aim to develop a method of access to enantiopure b-amino acids. Reactions conditions developed allowed to obtain an excellent diastereoselectivity from most dialkyl alkylidenemalonates
Jones, Catrin A. "The asymmetric synthesis of #alpha#-amino acids from imines." Thesis, Bangor University, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263167.
Повний текст джерелаLewis, Kirk Alexander. "Stereoselective synthesis using aminyl radicals derived from α-amino acids". Thesis, Loughborough University, 1997. https://dspace.lboro.ac.uk/2134/32976.
Повний текст джерелаBetit, Lyanne. "Derivatization of Azomethine Imines into beta-Aminocarbonyl Motifs." Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/32473.
Повний текст джерелаHartley, 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.
Повний текст джерелаКниги з теми "Imine acids"
Hartley, James Holroyd. Saccharide accelerated hydrolysis of boronic acid imines. Birmingham: University of Birmingham, 2000.
Знайти повний текст джерелаSantanilla, Alexander Buitrago. New Approaches Towards the Asymmetric Allylation of the Formyl and Imino Groups via Strained Silane Lewis Acids. [New York, N.Y.?]: [publisher not identified], 2013.
Знайти повний текст джерелаRosenthal, Gerald. Plant Nonprotein Amino and Imino Acids: Biological, Biochemical, and Toxicological Properties. Elsevier Science & Technology Books, 2012.
Знайти повний текст джерелаЧастини книг з теми "Imine acids"
Elford, Tim G., and Dennis G. Hall. "Catalytic Additions of Allylic Boronates to Carbonyl and Imine Derivatives." In Boronic Acids, 393–425. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527639328.ch8.
Повний текст джерелаBatey, Robert A. "Nucleophilic Addition Reactions of Aryl and Alkenylboronic Acids and Their Derivatives to Imines and Iminium Ions." In Boronic Acids, 279–304. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527606548.ch7.
Повний текст джерелаCavallini, Doriano, Giorgio Ricci, Silvestro Duprè, Laura Pecci, Mara Costa, Rosa M. Matarese, Bernardo Pensa, Antonio Antonucci, Sandro P. Solinas, and Mario Fontana. "Sulfur-containing cyclic ketimines and imino acids." In EJB Reviews 1991, 257–63. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-77200-9_19.
Повний текст джерелаTracey, M. R., R. P. Hsung, J. Antoline, K. C. M. Kurtz, L. Shen, B. W. Slafer, and Y. Zhang. "Imine/Enamide Rearrangement." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00408.
Повний текст джерелаCoates, C., J. Kabir, and E. Turos. "Ketene–Imine Cycloadditions." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00569.
Повний текст джерела"Reduction." In Biocatalysis in Organic Synthesis: The Retrosynthesis Approach, 73–112. The Royal Society of Chemistry, 2018. http://dx.doi.org/10.1039/bk9781782625308-00073.
Повний текст джерела"Coenzyme Forms of Vitamin B6." In The Chemical Biology of Human Vitamins, 193–227. The Royal Society of Chemistry, 2018. http://dx.doi.org/10.1039/bk9781788014649-00193.
Повний текст джерелаCoates, C., J. Kabir, and E. Turos. "Ester Enolate–Imine Cyclocondensations." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00574.
Повний текст джерелаPerst, H. "Connective Imine Formation by the Reaction of Thioketenes with Sulfur Diimides." In Three Carbon-Heteroatom Bonds: Thio-, Seleno-, and Tellurocarboxylic Acids and Derivatives; Imidic Acids and Derivatives; Ortho Acid Derivatives, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-023-00772.
Повний текст джерелаPerst, H. "Connective Imine Formation by Aza-Wittig Reaction of Iminophosphoranes or Related Compounds with Ketenes." In Three Carbon-Heteroatom Bonds: Thio-, Seleno-, and Tellurocarboxylic Acids and Derivatives; Imidic Acids and Derivatives; Ortho Acid Derivatives, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-023-00767.
Повний текст джерелаТези доповідей конференцій з теми "Imine acids"
Mallakpour, Shadpour. "Microstructure and properties of novel optically active poly(ester-imide)/TiO2 bionanocomposites containing natural amino acids moieties." In 2010 International Conference on Enabling Science and Nanotechnology (ESciNano). IEEE, 2010. http://dx.doi.org/10.1109/escinano.2010.5701084.
Повний текст джерелаPather, Kaveshree, Nuala A. Helsby, Brian D. Palmer, and Lai-Ming Ching. "Abstract 1555:In vitroandin vivoevaluation of analogs ofN-(o-carboxybenzoyl)glutamic acid imide, an active thalidomide metabolite." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-1555.
Повний текст джерелаWU, ZHIJIAN, FUQIANG BAN, and RUSSELL J. BOYD. "THEORETICAL STUDY ON THE REACTION MECHANISMS OF THE IMIDE FORMATION IN AN N-(O-CARBOXYBENZOYL)-L-AMINO ACID." In Proceedings of the International Symposium on Solid State Chemistry in China. WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812776846_0077.
Повний текст джерелаBigović, Miljan, Marija Kaluđerović, Jovana Jovanović, Haris Majstorović, and Milica Kosović-Perutović. "Synthesis of Schiff bases between some five-membered heterocyclic aldehydes and thiocarbohydrazide (TCH) and optimization of reaction conditions." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.435b.
Повний текст джерелаHaynes, A., and P. Gouma. "Nanoengineering Polyaniline for Advanced Chemosensing Applications." In ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-10310.
Повний текст джерелаLee, Chi-Hung, Jia-Ru Chen, Hung-Wei Shiu, Ko-Shan Ho, Shinn-Dar Wu, Kuo-Huang Hsieh, and Yen-Zen Wang. "Effect of Bridging Groups on Sulfonated Poly(Imide-Siloxane) for Application in Proton Exchange Membrane of Fuel Cells." In ASME 2008 6th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2008. http://dx.doi.org/10.1115/fuelcell2008-65155.
Повний текст джерела