Готові списки джерел за темами / Isoquinoline

Добірка наукової літератури з теми "Isoquinoline"

Автор: Grafiati
Опубліковано: 4 червня 2021
Оновлено: 30 липня 2024

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Статті в журналах з теми "Isoquinoline"

1

Mandrekar, Ketan S., and Santosh G. Tilve. "P4O10/TfOH mediated domino condensation–cyclization of amines with diacids: a route to indolizidine alkaloids under catalyst- and solvent-free conditions." RSC Advances 12, no. 28 (2022): 17701–5. http://dx.doi.org/10.1039/d2ra02534e.

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A highly efficient and direct methodology for the construction of pyrrolo[2,1-a]isoquinoline, pyrido[2,1-a]isoquinoline, and 12b-H and 12b-OH isoindolo[2,1-a]isoquinolinone alkaloids from commercially available synthons is devised.
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2

Yang, Chunmei, Guoqing Zhang, Senling Tang, Yang Pan, Huawu Shao, and Wei Jiao. "Dess–Martin Periodinane-Mediated Oxidative Coupling Reaction of Isoquinoline with Benzyl Bromide." Molecules 28, no. 3 (January 17, 2023): 923. http://dx.doi.org/10.3390/molecules28030923.

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Dess–Martin periodinane (DMP) is a broadly applicable oxidant in chemical synthesis. In this work, an efficient and convenient synthesis of N-substituted isoquinolinone derivatives mediated by DMP was achieved through the oxidative coupling reaction of functionalized isoquinoline with readily available benzyl bromide, which is a metal-free, mild, and practical method for synthesizing isoquinoline-1,3-dione or isoquinoline-1,3,4-trione derivatives in excellent yields. The H2O18-labeling experiment was performed to gain insight into the possible mechanism for this reaction.
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3

Koketsu, Mamoru, Amol Sonawane, Yunnus Shaikh, and Dinesh Garud. "Synthesis of Isoquinoline-Fused Quinazolinones through Ag(I)-Catalyzed Cascade Annulation of 2-Aminobenzamides and 2-Alkynylbenzaldehydes." Synthesis 51, no. 02 (September 21, 2018): 500–507. http://dx.doi.org/10.1055/s-0037-1610910.

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A new route for the expedient synthesis of a specific regioisomer of isoquinoline-fused quinazolinones is reported. Silver(I)-catalyzed cascade cyclization of 2-aminobenzamides and 2-alkynylbenzaldehydes followed by in situ oxidation gives 12-butyl- or 12-aryl-6H-isoquinolino[2,1-a]quinazolin-6-ones in 69–91% yields. The structure of the isoquinoline-fused quinazolinone was confirmed by X-ray crystallography analysis.
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4

Murtagh, Kevin, Brian A. Sweetman, and Patrick J. Guiry. "New chiral tridentate ligands for asymmetric catalysis." Pure and Applied Chemistry 78, no. 2 (January 1, 2006): 311–20. http://dx.doi.org/10.1351/pac200678020311.

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The synthesis of new tridentate, isoquinoline-derived ligands, involving successive Suzuki cross-coupling reactions, is described. We were able to resolve 1-[3-(2-hydroxy-phenyl)-isoquinolin-1-yl]-naphthalen-2-ol via molecular complexation with N-benzylcinchonidinium chloride, whereas 1,3-bis(2-hydroxy-naphthalen-1-yl)-isoquinoline was resolved by chromatographic separation of its epimeric camphorsulfonates. Their barrier to rotation about the central biaryl axis was evaluated via racemization studies. Application of enantiopure 1,3-bis(2-hydroxynaphthalen-1-yl)-isoquinoline in the addition of diethylzinc to aldehydes proceeded in moderate yield but without asymmetric induction. A new tridentate ligand, 4-tert-butyl-2-chloro-6-[1-(2-hydroxymethyl-naphthalen-1-yl)-isoquinolin-3-yl]-phenol, was prepared in good yield and resolved by semipreparative high-performance liquid chromatography (HPLC). Its application in the addition of diethylzinc to a range of aromatic aldehydes proceeded in near perfect enantioselectivities at low ligand loadings of 1 mol %.
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5

Zhang, Lujun, Wenfang Xiong, Biao Yao, Haitao Liu, Meng Li, Yu Qin, Yujian Yu, et al. "Facile synthesis of isoquinolines and isoquinoline N-oxides via a copper-catalyzed intramolecular cyclization in water." RSC Advances 12, no. 47 (2022): 30248–52. http://dx.doi.org/10.1039/d2ra06097c.

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6

Wu, Wei, Yan Wang, Jing Guo, Liu Cai, Yuan Chen, Yanmin Huang та Yungui Peng. "Asymmetric acyl-Mannich reaction of isoquinolines with α-(diazomethyl)phosphonate and diazoacetate catalyzed by chiral Brønsted acids". Chemical Communications 56, № 76 (2020): 11235–38. http://dx.doi.org/10.1039/d0cc03201h.

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7

Sloop, Joseph C. "Advances in the Preparation of Fluorinated Isoquinolines: A Decade of Progress." Journal of Chemistry 2017 (2017): 1–15. http://dx.doi.org/10.1155/2017/2860123.

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Heterocyclic molecules incorporating fluorinated isoquinoline components are found in many medicinally and agriculturally important bioactive products as well as industrially impactful materials. Within the past decade, a variety of isoquinolinic ring assembly techniques has enabled the introduction of diverse fluorine-containing functionalities which can enhance potential bioactivity and industrial utility. This review examines recent noncatalyzed and transition metal catalyzed synthetic approaches to the assembly of isoquinoline derivatives that are ring-fluorinated and/or result in the incorporation of fluorine-containing functional groups. Specifically, efficient synthetic methods and regioselectivity in the incorporation of functional groups into isoquinoline ring systems are examined.
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8

Li, Jiu-ling, Wei-ze Li, Ying-chun Wang, Qiu Ren, Heng-shan Wang, and Ying-ming Pan. "Palladium(ii)-catalyzed C–C and C–O bond formation for the synthesis of C1-benzoyl isoquinolines from isoquinoline N-oxides and nitroalkenes." Chemical Communications 52, no. 65 (2016): 10028–31. http://dx.doi.org/10.1039/c6cc03530b.

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9

An, Yuanyuan, Hongguang Xia, and Jie Wu. "Base-controlled [3+3] cycloaddition of isoquinoline N-oxides with azaoxyallyl cations." Chemical Communications 52, no. 68 (2016): 10415–18. http://dx.doi.org/10.1039/c6cc03650c.

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A base-controlled [3+3] cycloaddition reaction of isoquinoline N-oxides with azaoxyallyl cations is developed, leading to 1,11b-dihydro-[1,2,4]oxadiazino[3,2-a]isoquinolin-2(3H)-ones and 2-(isoquinolin-1-yloxy)acetamides, respectively. This transformation proceeds through an azaoxyallyl cation generated in situ from α-bromohydroxamate.
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10

Clark, Robin D., Jahangir, and James A. Langston. "Heteroatom-directed lateral lithiation: synthesis of isoquinoline derivatives from N-(tert-butoxycarbonyl)-2-methylbenzylamines." Canadian Journal of Chemistry 72, no. 1 (January 1, 1994): 23–30. http://dx.doi.org/10.1139/v94-005.

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Methodology for the preparation of isoquinoline derivatives from N-(tert-butoxycarbonyl)-2-methylbenzylamines (1) was developed. Conversion of 1 to the dilithio species followed by condensation with DMF afforded Boc-3-hydroxy-1,2,3,4-tetrahydroisoquinolines 3, which could be dehydrated to 1,2-dihydroisoquinolines 4. Hydrogenation of dihydro compounds 4 afforded the corresponding tetrahydroisoquinolines 5. Treatment of the dilithio species from 1 with N-methoxy-N-methylamides afforded ketones 14, which were converted to 3-substituted dihydro-isoquinoline 15, tetrahydroisoquinolines (16, 17), or isoquinolines (20).
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Дисертації з теми "Isoquinoline"

1

Berg, Michael Arthur George. "Studies in the stereoselective synthesis of 1,1-disubstituted 1,2,3,4-tetrahydroisoquinolines." Diss., This resource online, 1992. http://scholar.lib.vt.edu/theses/available/etd-10032007-171522/.

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2

Jones, Michael William Chemistry Faculty of Science UNSW. "Enhancing the cooperative binding properties of 1,1'-bis(1,2,3,4-tetrahydroisoquinolines)." Awarded by:University of New South Wales. School of Chemistry, 2005. http://handle.unsw.edu.au/1959.4/27400.

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The design of partially reduced 1,1'-bisisoquinoline derivatives was investigated with the aim of controlling the conformation about the C1-C1' axis. This would produce ligands with unusual but predictable ligand binding properties, particularly cooperativity. The introduction of ??-aminoalkyl, ??-azidoalkyl, ??-alkynyl and ??-alkenyl groups onto the nitrogens of the reduced bisisoquinoline core was conducted with the intention of broadening the scope of the ligand. Subsequent epoxidation, hydroboration and Huisgen 1,3-dipolar cycloaddition of terminal unsaturated groups and nucleophilic displacement of the chlorine of the corresponding known bischloroacetyl derivative afforded representative examples of new ligand types for future study. 1,1'-Bis(1,2,3,4-tetrahydro-6,7-dimethoxyisoquinoline) was found to readily condense with a wide range of aldehydes to give imidazolines and aspects of the rates of condensation were determined. Mono-alkyl bisisoquinolines were obtained efficiently by cleavage of the imidazolines through a newly defined treatment with sodium cyanoborohydride under acidic conditions. A procedure was developed whereby these two steps could be accomplished in a sequential one-pot process. The mono-alkyl compounds were further derivatized through acetylation, alkylation, sulfonylation and reductive alkylation. Synthetic strategies towards ??-excessive N-arenealkyl derivatives were established with the goal to create scaffolds for the coordination of ??-deficient systems, of which the X-ray crystal structures of three N-arenemethyl derivatives were elucidated. These are each closely related in conformation about the C1-C1' axis. Reaction of two examples of the N-arenealkyl compounds with copper(II) and palladium(II) chlorides, furnished the first known examples of this type of highly reduced 1,1'-bisisoquinoline-metal complex. Single crystal X-ray crystallography was used to analyse the structures of these complexes in the solid state. Preliminary physicochemical investigations were conducted with a view to determining the conformation of the molecules about the bisisoquinoline C1-C1' bond. The interaction of intermolecular N-aryl ??-excessive compounds with ??-deficient systems was found to result in minimal spectroscopic changes. Complementary intramolecular ??-excessive/??-deficient systems were found through fluorometric analysis to readily form charge transfer complexes. Finally, it was determined that the conformation of 1,1'-bis[2-(methoxy-18- crown-6)ethanoyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline] could be controlled by the simultaneous coordination of the termini of the diperchlorate salt of 1,3-diaminopropane to the crown ether moieties of the ligand. A range of new N-substituted bisisoquinolines have been synthesised and methods developed for determining interactions between parts of these molecules that through these physicochemical characteristics could allow monitoring of conformational behaviour in future studies. Keywords: 1,1'-bisisoquinoline, conformational analysis, supramolecular chemistry, functional ligands, metal complexes.
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3

Donaghy, Michael. "Studies in benzimidazo [2,1-a] isoquinoline chemistry." Thesis, Northumbria University, 2001. http://nrl.northumbria.ac.uk/1217/.

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Studies in Benzimidazo[2,1-a]isoquinoline Chemistry by Michael John Donaghy B. Sc. (Hons.) Ellipticine, a member of the pyrido[4,3-b]carbazole alkaloid family first isolated in 1959 from the leaves of the plant Ochrosia Elliptica has been shown to possess anti-cancer activity against various tumours. Ellipticine is thought to undergo biological oxidation to give the more active 9-hydroxyellipticine that is subsequently converted to a highly reactive quinone-imine intermediate. The quinone-imine is then thought to interact with bionucleophiles in the body promoting cell death. The aim of the project was to synthesise a series of benzimidazo[2,1-a]isoquinolines. The benzimidazo[2,1-c]isoquinolines were similar in general structure to ellipticines and should therefore undergo similar biological reactions. The target benzimidazo[2,1-a]isoquinolines have been screened to evaluate their ability to inhibit the enzyme topoisomerase II that is involved in DNA replication and ultimately cell reproduction. The target compounds have also been evaluated by the American National Cancer Institute.
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4

Clifton, Mary Jennifer. "Studies in stereoselective synthesis via reissert compound chemistry." Thesis, This resource online, 1991. http://scholar.lib.vt.edu/theses/available/etd-08222009-040256/.

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5

Guimond, Nicolas. "Part A: Rhodium-catalyzed Synthesis of Heterocycles / Part B: Mechanistic Studies on Tethering Organocatalysis Applied to Cope-type Alkene Hydroamination." Thèse, Université d'Ottawa / University of Ottawa, 2012. http://hdl.handle.net/10393/23222.

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The last decade has been marked by a large increase of demand for green chemistry processes. Consequently, chemists have focused their efforts on the development of more direct routes toward different classes of targets. In that regard catalysis has played a crucial role at enabling key bond formations that were otherwise inaccessible or very energy and resources consuming. The central theme of this body of work concerns the formation of C–N bonds, either through transition metal catalysis or organocatalysis. These structural units being highly recurrent in biologically active molecules, the establishment of more efficient routes for their construction is indispensable. The first part of this thesis describes a new method for the synthesis of isoquinolines from the oxidative coupling/annulation of alkynes with N-tert-butyl benzaldimines via Rh(III) catalysis (Chapter 2). Preliminary mechanistic investigations of this system pointed to the involvement of Rh(III) in the C–H bond cleavage step as well as in the C–N bond reductive elimination that provides the desired heterocycle. Following this oxidative process, a Rh(III)-catalyzed redox-neutral approach to isoquinolones from the reaction of benzhydroxamic acids with alkynes is presented (Chapter 3). The discovery that an N–O bond contained in the substrate can act as an internal oxidant was found to be very enabling. Indeed, it allowed for milder reaction conditions, broader scope (terminal alkyne and alkene compatible) and low catalyst loadings (0.5 mol%). Mechanistic investigations on this system were also conducted to identify the nature of the C–N bond formation/N–O bond cleavage as well as the rate-determining step. The second part of this work presents mechanistic investigations performed on a recently developed intermolecular hydroamination reaction catalyzed through tethering organocatalysis (Chapter 4). This transformation operates via the reversible covalent attachment of two reactants, a hydroxylamine and an allylamine, to an aldehyde catalyst by the formation of a mixed aminal. This allows a difficult intermolecular Cope-type hydroamination to be performed intramolecularly. The main kinetic parameters associated with this reaction were determined and they allowed the generation of a more accurate catalytic cycle for this transformation. Attempts at developing new families of organocatalysts are also discussed.
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6

Ford, Alan John. "Synthesis of substituted isoquinoline ligands for homogeneous catalysis." Thesis, University of Hull, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.361496.

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7

Muzanila, Charles Nobert. "Heterocyclic transformations involving #DELTA#'2-oxazolines and 1,2-benzisoxazoles." Thesis, University of Salford, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327958.

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8

Hamilton, Lynne. "Synthesis, stereochemistry and reactions of quinoline, isoquinoline and acridine metabolites." Thesis, Queen's University Belfast, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334710.

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9

Streetley, Guy Bradwell. "New approaches for the asymmetric synthesis of pyrroloisoquinoline and isoquinoline alkaloids." Thesis, Loughborough University, 2006. https://dspace.lboro.ac.uk/2134/34917.

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Pyrroloisoquinoline (n = 1) and the pyridoisoquinoline (n = 2) ring systems (2) are found to be the major structural motif of the Erythrina and the protoberberine group of alkaloids, respectively. We have recognised that suitable bicyclic lactams (1) could act as precursors, in an intramolecular N-acyliminium ion-mediated cyclisation, resulting in a stereoselective approach to the core of the Erythrina and protoberberine ring systems. [Illustration omitted.] Access to the tetracyclic core of the Erythrina alkaloids (3) through the application of N-acyliminium ion chemistry is well established within our group. This has been demonstrated in a formal asymmetric synthesis of both enantiomers of the Erythrina alkaloid, 3- demethoxyerythratidinone (4), and described in this thesis. [Illustration omitted.] Our investigations have also involved the manipulation of this methodology toward the synthesis of the Erythrina alkaloid (-)-erysotrine (5) and the protoberberine alkaloid (-)-xylopinine (6).
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10

Chow, Yit Lai. "Caenorhabditis elegans as a whole organism screening system for isoquinoline alkaloid bioactivities." 京都大学 (Kyoto University), 2014. http://hdl.handle.net/2433/188834.

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Книги з теми "Isoquinoline"

1

D, Phillipson J., Roberts M. F, Zenk M. H. 1933-, and Phytochemical Society of Europe, eds. The Chemistry and biology of isoquinoline alkaloids. Berlin: Springer-Verlag, 1985.

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2

Bentley, K. W. The Isoquinoline alkaloids. Amsterdam, The Netherlands: Harwood Academic Pub., 1998.

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3

Phillipson, J. David, Margaret F. Roberts, and M. H. Zenk, eds. The Chemistry and Biology of Isoquinoline Alkaloids. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-70128-3.

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4

1948-, Coppola Gary M., and Schuster Herbert F. 1949-, eds. Isoquinolines. New York: Wiley, 1995.

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5

Antkiewicz-Michaluk, Lucyna, and Hans Rommelspacher, eds. Isoquinolines And Beta-Carbolines As Neurotoxins And Neuroprotectants. Boston, MA: Springer US, 2012. http://dx.doi.org/10.1007/978-1-4614-1542-8.

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6

The Chemistry of Heterocyclic Compounds, Isoquinolines (Chemistry of Heterocyclic Compounds: A Series Of Monographs). Wiley-Interscience, 1995.

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7

Rahman, A. U. Isoquinoline Alkaloids. Elsevier Science, 1994.

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8

Chemistry and Biology of Isoquinoline Alkaloids. Island Press, 1985.

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9

Schuster, Herbert F., and Gary M. Coppola. Isoquinolines, Part 3. Wiley & Sons, Incorporated, John, 2009.

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10

(Editor), F. G. Kathawala, Gary M. Coppola (Editor), and Herbert F. Schuster (Editor), eds. The Chemistry of Heterocyclic Compounds, Isoquinolines (Chemistry of Heterocyclic Compounds: A Series Of Monographs). 2nd ed. Wiley-Interscience, 1990.

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Частини книг з теми "Isoquinoline"

1

Niwa, Toshimitsu, Mitsuharu Kajita, and Toshiharu Nagatsu. "Isoquinoline Derivatives." In Pharmacology of Endogenous Neurotoxins, 3–23. Boston, MA: Birkhäuser Boston, 1998. http://dx.doi.org/10.1007/978-1-4612-2000-8_1.

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2

Nagatsu, Toshiharu. "Isoquinoline Neurotoxins." In Neurotoxic Factors in Parkinson’s Disease and Related Disorders, 69–76. Boston, MA: Springer US, 2000. http://dx.doi.org/10.1007/978-1-4615-1269-1_7.

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3

Vogt, J. "715 C9H7N Isoquinoline." In Asymmetric Top Molecules. Part 3, 239. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14145-4_137.

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4

Wohlfarth, Ch. "Viscosity of isoquinoline." In Supplement to IV/18, 560. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_313.

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5

Li, Jie Jack. "Pictet-Gams isoquinoline synthesis." In Name Reactions, 312–13. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_233.

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6

dos Santos, Anderson R., and Nelissa P. Vaz. "Isoquinoline Alkaloids and Chemotaxonomy." In Sustainable Development and Biodiversity, 167–93. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-30746-2_8.

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7

Wohlfarth, Ch. "Dielectric constant of isoquinoline." In Supplement to IV/6, 452. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_278.

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8

Li, Jie Jack. "Pictet–Gams isoquinoline synthesis." In Name Reactions, 478–79. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_214.

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9

Seigler, David S. "Isoquinoline and Benzylisoquinoline Alkaloids." In Plant Secondary Metabolism, 578–616. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4913-0_32.

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10

Li, Jie Jack. "Pictet-Gams isoquinoline synthesis." In Name Reactions, 282. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_222.

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Тези доповідей конференцій з теми "Isoquinoline"

1

Wang Guanghua, Yang Shuqin, Li Wenbing, Lei Qi, Liu Xueqin, Liu Wenmin, Liu Qi, Liu Tiejun, and Jiang Lijuan. "Isolation and characterization of isoquinoline-degrading strain Y-4." In Environment (ICMREE). IEEE, 2011. http://dx.doi.org/10.1109/icmree.2011.5930957.

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2

O'Donnell, Ryan M., Autumn E. Moore, Jianmin Shi, Trenton R. Ensley, Michael J. Ferry, Neal K. Bambha, and William M. Shensky. "Iridium complexes containing nitro-derivatized isoquinoline ligands for photonic applications." In Organic Photonic Materials and Devices XXI, edited by Christopher E. Tabor, François Kajzar, and Toshikuni Kaino. SPIE, 2019. http://dx.doi.org/10.1117/12.2508772.

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3

Gumus, Aysegul, Selcuk Gumus, and Duygu Yenidede. "Isoquinoline-substituted hybrid compounds: synthesis and computational studies." In The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a036.

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4

Silva, Wanderson Amaral da, Vinícius Rangel Campos, Angela Cristina P. B. dos Santos, Alessandro K. Jordão, Vitor F. Ferreira, Maria Cecília B. V. de Souza, and Anna Claudia Cunha. "The Ultrasound-accelerated Synthesis of New 7- Aminocarbohydrate-isoquinoline-5,8-quinone Derivatives." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0253-2.

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5

Penkevich, N. A., Yu P. Slapovskaya, A. A. Neveshkin, D. A. Zayarsky, and V. B. Bayburin. "Optical spectroscory of isoquinoline-1-carboxylate europium with sodium in various solvents." In 2014 International Conference on Actual Problems of Electron Devices Engineering (APEDE). IEEE, 2014. http://dx.doi.org/10.1109/apede.2014.6958228.

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6

Hung, J., J. Castillo, I. Laboren, M. Rodríguez, and M. Hassegawa. "Measurement of antiphotooxidative properties of isoquinoline alkaloids using transient thermal lens spectroscopy." In Optics East 2005, edited by Mostafa Analoui and David A. Dunn. SPIE, 2005. http://dx.doi.org/10.1117/12.630074.

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7

Couture, Axel, Pierre Grandclaudon, Eric Deniau, Stéphane Lebrun, and Mélanie Dubois. "Alternative synthetic approaches to biologically active indeno[1,2-c]isoquinoline-5,11-diones." In The 15th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00569.

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8

Cahlíková, L., A. Al Mamun, O. Janďourek, K. Sobolová, J. Křoustková, J. Korábečný, R. Peřinová, and K. Hradiská Breiterová. "Short Lecture “Isoquinoline alkaloids and their derivatives as a new class of antimycobacterial drugs”." In GA – 70th Annual Meeting 2022. Georg Thieme Verlag KG, 2022. http://dx.doi.org/10.1055/s-0042-1758970.

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9

Vasilopoulos, S., I. Giannenas, K. Bitchava, M. Stefanakis, P. Chantzi, S. Dokou, A. Efstathiou, et al. "Effect of isoquinoline alkaloids on trout performance antioxidant status and filet fatty acid profile." In GA – 70th Annual Meeting 2022. Georg Thieme Verlag KG, 2022. http://dx.doi.org/10.1055/s-0042-1759319.

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Wang, Lin, Lijuan Sun, and Yongmei Li. "Promotive Effect of Pyridine on the Biodegradation of Isoquinoline by Activated Sludge under Denitrifying Conditions." In 2009 3rd International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2009. http://dx.doi.org/10.1109/icbbe.2009.5163252.

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Звіти організацій з теми "Isoquinoline"

1

Blackwood, D. J., and S. Pons. An In Situ Surface Fourier Transform Infrared Study of the Adsorption of Isoquinoline at a Stationary Mercury Electrode. Fort Belvoir, VA: Defense Technical Information Center, July 1988. http://dx.doi.org/10.21236/ada201685.

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2

Beasley, Jonathan. Synthesis of heterocycles: Indolo (2,1-a) isoquinolines, renewables, and aptamer ligands for cellular imaging. Office of Scientific and Technical Information (OSTI), January 2013. http://dx.doi.org/10.2172/1082980.

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