Gotowa bibliografia na temat „Isochromans”
Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych
Spis treści
Zobacz listy aktualnych artykułów, książek, rozpraw, streszczeń i innych źródeł naukowych na temat „Isochromans”.
Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.
Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.
Artykuły w czasopismach na temat "Isochromans"
Hamada, Shohei, Kyoko Yano, Ayano Ohshimo, Elghareeb E. Elboray, Yusuke Kobayashi i Takumi Furuta. "Oxidative C–N Bond Formation of Isochromans Using an Electronically Tuned Nitroxyl Radical as Catalyst". SynOpen 08, nr 02 (maj 2024): 125–29. http://dx.doi.org/10.1055/s-0040-1720118.
Pełny tekst źródłaLiu, Shiyao, Kazunari Nakajima i Yoshiaki Nishibayashi. "Copper-catalysed enantioselective intramolecular etherification of propargylic esters: synthetic approach to chiral isochromans". RSC Advances 9, nr 33 (2019): 18918–22. http://dx.doi.org/10.1039/c9ra03880a.
Pełny tekst źródłaTrefiletti, Giuliana, Anna Rita Togna, Valentina Latina, Carolina Marra, Marcella Guiso i Giuseppina I. Togna. "1-Phenyl-6,7-dihydroxy-isochroman suppresses lipopolysaccharide-induced pro-inflammatory mediator production in human monocytes". British Journal of Nutrition 106, nr 1 (27.01.2011): 33–36. http://dx.doi.org/10.1017/s0007114510005763.
Pełny tekst źródłaUNTERHALT, B., i R. JOESTINGMEIER. "ChemInform Abstract: New Substituted Isochromans." ChemInform 28, nr 1 (4.08.2010): no. http://dx.doi.org/10.1002/chin.199701169.
Pełny tekst źródłaVerma, Ashish Kumar, Ande Chennaiah, Sateesh Dubbu i Yashwant D. Vankar. "Stereoselective synthesis of sugar-fused (or 1,2-annulated) isochromans and isochromanones by using oxa-Pictet–Spengler reaction". Organic & Biomolecular Chemistry 16, nr 37 (2018): 8258–62. http://dx.doi.org/10.1039/c8ob01698d.
Pełny tekst źródłaThatikonda, Thanusha, Siddharth K. Deepake, Pawan Kumar i Utpal Das. "α-Angelica lactone catalyzed oxidation of benzylic sp3 C–H bonds of isochromans and phthalans". Organic & Biomolecular Chemistry 18, nr 21 (2020): 4046–50. http://dx.doi.org/10.1039/d0ob00729c.
Pełny tekst źródłaNickerson, Leslie A., Benjamin D. Bergstrom, Mingchun Gao, Yuan-Shin Shiue, Croix J. Laconsay, Matthew R. Culberson, Walker A. Knauss, James C. Fettinger, Dean J. Tantillo i Jared T. Shaw. "Correction: Enantioselective synthesis of isochromans and tetrahydroisoquinolines by C–H insertion of donor/donor carbenes". Chemical Science 11, nr 19 (2020): 5113. http://dx.doi.org/10.1039/d0sc90081h.
Pełny tekst źródłaUnterhalt, B., i U. Heppert. "ChemInform Abstract: Isochromans Related to Fluoxetin." ChemInform 32, nr 38 (24.05.2010): no. http://dx.doi.org/10.1002/chin.200138108.
Pełny tekst źródłaZhu, Zhengbo, Alafate Adili, Chenfei Zhao i Daniel Seidel. "Catalytic Enantioselective Approaches to the oxa-Pictet–Spengler Cyclization and Other 3,6-Dihydropyran-Forming Reactions". SynOpen 03, nr 03 (lipiec 2019): 77–90. http://dx.doi.org/10.1055/s-0039-1690686.
Pełny tekst źródłaYang, Guoping, Ke Li, Kai Zeng, Yijin Li, Tao Yu i Yufeng Liu. "Heteropolyacid ionic liquid heterogeneously catalyzed synthesis of isochromans via oxa-Pictet–Spengler cyclization in dimethyl carbonate". RSC Advances 11, nr 18 (2021): 10610–14. http://dx.doi.org/10.1039/d1ra01004b.
Pełny tekst źródłaRozprawy doktorskie na temat "Isochromans"
Joll, Cynthia Ann. "The asymmetric synthesis of isochromans related to the aphid pigments". Thesis, Joll, Cynthia Ann (1995) The asymmetric synthesis of isochromans related to the aphid pigments. PhD thesis, Murdoch University, 1995. https://researchrepository.murdoch.edu.au/id/eprint/51655/.
Pełny tekst źródłaMuller, Cyprien. "Supramolecular catalysis and vibrational strong coupling : how to influence chemical reactivity ?" Electronic Thesis or Diss., Strasbourg, 2024. http://www.theses.fr/2024STRAF014.
Pełny tekst źródłaHow can we influence chemical reactivity? Throughout this thesis, I attempted to answer this question by exploring the frontier between chemistry and physics.First, I took advantage of solvent 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) which often unlocks exotic reactivity that can be explained by its extraordinary physical properties. These properties make of HFIP a veritable supramolecular matrix, which allowed the development of a new method for the synthesis of densely functionalized isochromans. This method displayed unprecedented generality, simplicity, and practicality on the way to this pharmacologically important motif.Second, I investigated how light-matter hybridization, accessed through Vibrational Strong Coupling (VSC) could alter the kinetics of some chemical reactions. In practice, by placing different reactants between two mirrors, I studied the impact of VSC on nucleophilicity, as well as on Diels-Alder reactivity
Fronert, Jeanne Katrin [Verfasser]. "Organokatalytische asymmetrische Synthesen von Dihydrobenzofuranen und Isochroman-1-onen / Jeanne Katrin Fronert". Aachen : Hochschulbibliothek der Rheinisch-Westfälischen Technischen Hochschule Aachen, 2015. http://d-nb.info/1080490825/34.
Pełny tekst źródłaHabert, Loïc. "Synthèse et étude de la réactivité d'ynamides. Application pour la synthèse de composés azotés d'intérêts biologiques". Thesis, Orléans, 2018. http://www.theses.fr/2018ORLE2065.
Pełny tekst źródłaThe constant demand for original small molecule collections with promesing therapeutic potential have required the development of new and efficient synthetic methods. Given the nitrogen ubiquity in nature and in life sciences, the aim of this work is the development of original heterocyclic building blocks, originated from the functionalization of ynamide frameworks. Our goal was to study the reactivity of ynamides in order to synthesize from a common skeleton small library of nitrogen or oxygen compounds with biological relevance. The implementation of a new innovative methodology has been necessary, while trying to adhere to the following principles: atom economy, catalytic reaction, fast synthesis in minimal steps, and control of chemo- and regioselectivity.Firstly, we studied the carbozincation reaction of ynamides allowing access to several substituted enamides. Subsequently, cycloisomerization reaction of yne-carbamates has allowed us the development of two novels methodologies using zinc (II) or rhodium (II) salts, which provide access to oxazolone scaffolds. Our research has been studying the keteniminium ion intermediates accessible via an acid activation of ynamide. The development of two methods for the 3-amino-isocoumarin core was achieved via addition of Lewis or Brønsted acid or via electrophilic cyclization. Finally, a tandem coupling / cycloisomerization / nucleophilic addition reaction was carried out in order to prepare 1H-isochromene
Lewis, Shane E. "Development of a Three Step Cascade Synthesis of 2,4-Dihydro-1H-benzo[f]isochromenes". W&M ScholarWorks, 2015. https://scholarworks.wm.edu/etd/1539626965.
Pełny tekst źródłaCoelho, Paulo. "Etude de la diastereoselectivite des reactions intramoleculaires de composes presentant un atome de silicium chiral. Synthese de derives de 4-silatetrahydro-isochroman-1-ones, de 4-sila-2h-isoquinolein-1-ones et de silacycloalcanes". Paris 11, 1995. http://www.theses.fr/1995PA112069.
Pełny tekst źródłaMariaule, Gaëlle. "Accès original aux hétérocycles par la catalyse organométallique : développement de nouveaux inhibiteurs de kinases". Thesis, Paris 5, 2014. http://www.theses.fr/2014PA05P612/document.
Pełny tekst źródłaMy thesis proJect is organized around two main topics having in common organometallic chemistry and the synthesis of heterocycles.Firstly, we were interested in a methodology for the synthesis of tetrahydrocyclopenta[c]acridines. These compounds are synthesized in three steps from various quinolines. The key step is a cobalt-Catalyzed intramolecular Pauson-Khand reaction. Some compounds of this family exhibit selective Cyclin Dependent Kinases (CDKs) inhibition, particulary against CDK2, in the submicromolar range. A hit compound has been identified, and then using data from co-Crystallization with CDK2 and molecular modeling, followed by the study of structure-Activity relationships, the rational design of a second generation of molecules has been investigated. The most advanced compound has an IC50 of 300 nM against CDK2/cyclin A with an excellent metabolic profile. In the second axis of research, we have studied and developed a new silver-Catalyzed tandem addition/cyclization reaction with carbon nucleophiles. The systems studied are (hetero)aromatics compounds having an aldehyde group and in ortho-Position an alkynyl group. The synthetic strategy leads to 1H-Isochromene derivatives by creating two new bonds. A thorough study of the tandem reaction allowed us to obtain a wide range of isochromene derivatives, highlighting the influence of different substituents carried by the alkyne group or on the (hetero)aromatic substrates; and also to investigate the use of different carbon nucleophiles (alkynes, aromatics and heteroaromatics). The limitations of the tandem reaction have also been identified
Gorgoi, Mihaela. "Electronic Properties of Phthalocyanines Deposited on H-Si(111)". Doctoral thesis, Universitätsbibliothek Chemnitz, 2007. http://nbn-resolving.de/urn:nbn:de:swb:ch1-200700213.
Pełny tekst źródłaIn the context of this work four Phthalocyanine were studied: Metal-free Phthalocyanine (H2Pc), Copper Phthalocyanine (CuPc) and fluorine-substituted Phthalocyanine (F4CuPc and F16CuPc). The goal of this work is the electronic and chemical characteristics of the interfaces. The molecules were deposited by organic molecular beam deposition (OMBD) in the ultra high vacuum on hydrogen-passivated Si(111)-Substrate. Surface sensitive techniques such as photoemission spectroscopy (PES), bremsstrahlung isochromate spectroscopy (BIS or IPES - inverse photoemission spectroscopy) and near edge X-ray absorption fine structure spectroscopy (NEXAFS) were used for characterisation. Theoretical computations by density functional theory methods were employed, in order to assign different components in PES and IPES. The energy level alignment at the organic/H-Si interface, as well as the transport gap of H2Pc, CuPc, F4CuPc and F16CuPc were determined by PES and IPES. The NEXAFS measurements determine the exact molecular orientation with respect to the substrate. The evaluation of the data showed different molecular orientation in the thin and thick films. This change was correlated with the band bending like behaviours that emerged at these interfaces. In addition to the band bending like behaviour, the interfaces show also an interface dipole which is driven by the work function difference between the contact materials. The influence of the degree of fluorination is confirmed in the similar increase of the EA, WF and IE. The electronic properties of metal/organic layer interfaces and of organic layer under oxygen influence were examined by PES and IPES. The Ag/Pc interfaces show a mixture of HOMO-LUMO shifts and interface dipole formation. A charge transfer complex is formed in the case of Ag/H2Pc and Ag/F16CuPc interfaces. Ag is physisorbed atop the CuPc. Charge transfers from F4CuPc to Ag creating a continuous n-type doping at the interface. Similar to the Pc/H-Si interfaces the interface dipoles found here show a linear dependence on the EA, WF and IE and can be predicted by the difference in the work functions. The data evaluation of oxygen exposed thick films determined two groups of behaviours. The weak interaction group is represented by H2Pc and F4CuPc, Pcs on which oxygen is physisorbed. The strong interaction group contains the other two molecules CuPc and F16CuPc. CuPc forms a charge transfer complex with oxygen and on top of F16CuPc a polarized layer is formed
Gina, Ervin. "Implementation and Optimization of an Inverse Photoemission Spectroscopy Setup". Scholar Commons, 2012. http://scholarcommons.usf.edu/etd/4050.
Pełny tekst źródłaSenanayake, Badra Sriyani. "Approaches to natural isochromans by isomerisation of aryldioxolanes". Phd thesis, 1992. http://hdl.handle.net/1885/138963.
Pełny tekst źródłaCzęści książek na temat "Isochromans"
Lavine, Barry K., i Collin White. "Odor-Structure Relationship Studies of Indan, Tetralin, and Isochroman Musks". W ACS Symposium Series, 333–59. Washington, DC: American Chemical Society, 2015. http://dx.doi.org/10.1021/bk-2015-1191.ch023.
Pełny tekst źródłaFuggle, John C. "Bremsstrahlung isochromat spectroscopy (BIS or High-Energy Inverse Photoemission)". W Topics in Applied Physics, 307–37. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/3540541624_20.
Pełny tekst źródłaFauszt, I., A. Fehér, Gy Horváth, A. Juhász, E. Széll i S. Bajusz. "Facile synthesis of 1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid, a constrained phenylglycine and its oxa analog, isochromane-1-carboxylic acid". W Peptides 1994, 678–79. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-1468-4_311.
Pełny tekst źródłaFortuné, Danielle, i Bruno Deshoullières. "Modelling of Sliding Wave Phenomenon, on the Contact Boundary between Two Bodies, by the Boundary Integral Element Method: Numerical Visualization of Isochroms". W Contact Mechanics, 267–70. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4615-1983-6_36.
Pełny tekst źródła"Olive Oil Hydroxy-Isochromans". W Olive Oil, 207–14. CRC Press, 2008. http://dx.doi.org/10.1201/9781420059946-13.
Pełny tekst źródłaGuiso, Marcella, Giuliana Trefiletti i Giuseppina Togna. "Olive Oil Hydroxy-Isochromans". W Olive Oil, 193–200. CRC Press, 2008. http://dx.doi.org/10.1201/9781420059946.ch9.
Pełny tekst źródłaNógrádi, M. "By Oxidative Fragmentation of 1-2-Benzopyrans (Isochromans)". W Six-Membered Hetarenes with One Chalcogen, 1. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-014-00146.
Pełny tekst źródłaFreeman, R. "Spin choreography". W Pulsed Magnetic Resonance: NMR, ESR, and Optics, 219–41. Oxford University PressOxford, 1992. http://dx.doi.org/10.1093/oso/9780198539629.003.0010.
Pełny tekst źródłaRiviere, J. C. "Electron excitation: inverse photoemission spectroscopy (IPES)". W Surface Analytical Techniques, 193–209. Oxford University PressOxford, 1990. http://dx.doi.org/10.1093/oso/9780198513704.003.0007.
Pełny tekst źródłaHillebrecht, F. U., i M. Campagna. "Chapter 70 Bremsstrahlung isochromat spectroscopy of alloys and mixed valent compounds". W High Energy Spectroscopy, 425–51. Elsevier, 1987. http://dx.doi.org/10.1016/s0168-1273(87)10012-8.
Pełny tekst źródłaStreszczenia konferencji na temat "Isochromans"
"SEMI-EXPERIMENTAL INVESTIGATION OF COMPOUND 1H,3HBENZO[DE]ISOCHROMENE-1,3-DIONE". W 2nd International Conference on Contemporary Academic Research ICCAR 2023. All Sciences Academy, 2023. http://dx.doi.org/10.59287/as-proceedings.191.
Pełny tekst źródłaC.T., Samlan, Dinesh N. Naik i Nirmal K. Viswanathan. "Separating Isogyres and Isochromates of a Uniaxial Crystal using Fourier Fringe Analysis". W International Conference on Fibre Optics and Photonics. Washington, D.C.: OSA, 2016. http://dx.doi.org/10.1364/photonics.2016.th3a.4.
Pełny tekst źródłaJackson, Warren B. "Electronic Structure of Crystalline and Amorphous Semiconductors and Heterojunctions Using Bremsstrohlung Isochromat Spectroscopy". W 1986 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 1986. http://dx.doi.org/10.7567/ssdm.1986.d-11-1.
Pełny tekst źródłaRaporty organizacyjne na temat "Isochromans"
Tobin, J., M. Butterfield, N. Teslich, A. Bliss, B. Chung, J. Gross, A. McMahan i A. Schwartz. Nano-focused Bremstrahlung Isochromat Spectroscopy (nBIS) Determination of the Unoccupied Electronic Structure of Pu. Office of Scientific and Technical Information (OSTI), grudzień 2006. http://dx.doi.org/10.2172/898443.
Pełny tekst źródła