Relevant bibliographies by topics / Metal diketonate

Academic literature on the topic 'Metal diketonate'

Author: Grafiati
Published: 10 December 2022
Last updated: 29 January 2023

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Journal articles on the topic "Metal diketonate"

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Berry, A. D., R. T. Holm, M. Fatemi, and D. K. Gaskill. "OMCVD of thin films from metal diketonates and triphenylbismuth." Journal of Materials Research 5, no. 6 (June 1990): 1169–75. http://dx.doi.org/10.1557/jmr.1990.1169.

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Films containing the metals copper, yttrium, calcium, strontium, barium, and bismuth were grown by organometallic chemical vapor deposition (OMCVD). Depositions were carried out at atmospheric pressure in an oxygen-rich environment using metal beta-diketonates and triphenylbismuth. The films were characterized by Auger electron spectroscopy, Nomarski and scanning electron microscopy, and x-ray diffraction. The results show that films containing yttrium consisted of Y2O3 with a small amount of carbidic carbon, those with copper and bismuth were mixtures of oxides with no detectable carbon, and those with calcium, strontium, and barium contained carbonates. Use of a partially fluorinated barium beta-diketonate gave films of BaF2 with small amounts of BaCO3.
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Cavell, KJ. "Metal Chelate Systems as Catalysts for Olefin and Carbon Monoxide Conversion Reactions." Australian Journal of Chemistry 47, no. 5 (1994): 769. http://dx.doi.org/10.1071/ch9940769.

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The application of non-phosphine-based chelating ligands in homogeneous catalyst systems is a surprisingly recent and relatively unexplored area of research. Chelating ligands can concurrently stabilize intermediates, control catalyst activity and direct the product distribution far more effectively than monodentate ligands. In this review our studies with catalyst systems containing chelate ligands primarily of the β-diketonate type [dithio-β-diketonate (sacsac); monothio-β-diketonate (sacac); and imino β-diketonate (nacac) ligands] is discussed. Examples of the catalyst systems show enzyme-like superactivity. Studies modelling these catalyst systems have provided valuable information relating the effects of ligand modifications to reaction pathways and to activities. Our most recent investigations of simple chelating ligands based on picolinic acid are also discussed. Studies modelling CO/ethene insertion/elimination with extremely labile alkylplatinum picolinate complexes led to the development of new single-component nickel oligomerization catalysts.
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Blasi, Delia, Pierluigi Mercandelli, and Lucia Carlucci. "Supramolecular Frameworks and a Luminescent Coordination Polymer from New β-Diketone/Tetrazole Ligands." Inorganics 10, no. 4 (April 18, 2022): 55. http://dx.doi.org/10.3390/inorganics10040055.

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Mixed multidentate linkers with donor groups of different types can be fruitfully exploited in the self-assembly of coordination polymers (CPs) and Metal-Organic Frameworks (MOFs). In this work we develop new ligands containing a β-diketone chelating functionality, to better control the stereochemistry at the metal center, and tetrazolyl multidentate bridging groups, a combination not yet explored for networking with metal ions. The new ligands, 1,3-bis(4-(1H-tetrazol-5-yl)phenyl)-1,3-propanedione (H3L1) and 1-phenyl-3-(4-(1H-tetrazol-5-yl)phenyl)-1,3-propanedione (H2L2), are synthesized from the corresponding nitrile precursors by [2+3] dipolar cycloaddition of azide under metal-free catalytic conditions. Crystal structure analysis evidences the involvement of tetrazolyl fragments in multiple hydrogen bonding giving 2D and 1D supramolecular frameworks. Reactivity of the new ligands with different metal salts indicates good coordinating ability, and we report the preparation and structural characterization of the tris–chelate complex [Fe(HL1)3]3− (1) and the homometallic 2D CP [ZnL2(DMSO)] (2). In compound 1 only the diketonate donor is used, whereas the partially deprotonated tetrazolyl groups are involved in hydrogen bonding, giving rise to a 2D supramolecular framework of (6,3)IIa topological type. In compound 2 the ligand is completely deprotonated and uses both the diketonate donor (chelating) and the tetrazolate fragment (bridging) to coordinate the Zn(II) ions. The resulting neutral 2D network of sql topology shows luminescence in the solid state, which is red shifted with respect to the free ligand. Interestingly, it can be easily exfoliated in water to give a luminescent colloidal solution.
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Krajewski, Sebastian M., Aaron S. Crossman, Eser S. Akturk, Tim Suhrbier, Steven J. Scappaticci, Maxwell W. Staab, and Michael P. Marshak. "Sterically encumbered β-diketonates and base metal catalysis." Dalton Transactions 48, no. 28 (2019): 10714–22. http://dx.doi.org/10.1039/c9dt02293g.

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Walczak, Anna, Gracjan Kurpik, and Artur R. Stefankiewicz. "Intrinsic Effect of Pyridine-N-Position on Structural Properties of Cu-Based Low-Dimensional Coordination Frameworks." International Journal of Molecular Sciences 21, no. 17 (August 26, 2020): 6171. http://dx.doi.org/10.3390/ijms21176171.

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Metal-organic assemblies have received significant attention for catalytic and other applications, including gas and energy storage, due to their porosity and thermal/chemical stability. Here, we report the synthesis and physicochemical characterization of three metallosupramolecular assemblies consisting of isomeric ambidentate pyridyl-β-diketonate ligands L1–L3 and Cu(II) metal ions. It has been demonstrated that the topology and dimensionality of generated supramolecular aggregates depend on the location of the pyridine nitrogen donor atom in L1–L3. This is seen in characterization of two distinct 2D polymeric assemblies, i.e., [Cu(L1)2]n and [Cu(L2)2]n, in which both β-diketonate and pyridine groups are coordinated to the Cu(II) center, as well as in characterization of the mononuclear 1D complex Cu(L3)2, in which the central atom is bound only by two β-diketonate units.
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Wang, Hongmei, Zulei Zhang, Hailong Wang, Liping Guo, and Lei Li. "Metal β-diketonate complexes as highly efficient catalysts for chemical fixation of CO2 into cyclic carbonates under mild conditions." Dalton Transactions 48, no. 42 (2019): 15970–76. http://dx.doi.org/10.1039/c9dt03584b.

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Ivakha, Nadiia, Oleksandra Berezhnytska, Oleksandr Rohovtsov, Olena Trunova, and Serhii Smola. "INVESTIGATION OF NEW POLYMER COMPLEXES BASED ON Yb(III) β-DIKETONATES." Ukrainian Chemistry Journal 88, no. 5 (June 24, 2022): 3–14. http://dx.doi.org/10.33609/2708-129x.88.05.2022.3-14.

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The metal polymers based on mono- and heteroligand β-diketonate complexes of Yb(III) with 2,7-dimethyl-octen-1-dione-3,5, 2,6-dimethyl-heptene-1-dione-3, 5 and with phenanthroline was synthesized. It has been defined that the coordination environment of the central ion remains unchanged during radical polymerization. The shape and position of the bands in the electronic absorption spectra are similar to the corresponding monomeric β-diketonate metal complexes, and slight shifts indicate deformation of the elementary unit of the metal polymer during the formation of the polymer chain. It is shown that the polymerization process lead to an increasing in the thermal stability of polymer complexes in comparison with monomeric analogues. An increase in the emission of metal polymers in comparison with monomeric complexes was established by the method of luminescent spectroscopy, which is due to energy, steric, and structural-mechanical factors.
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Marciniak, Bronislaw, and Gonzalo E. Buono-Core. "Photochemical properties of 1,3-diketonate transition metal chelates." Journal of Photochemistry and Photobiology A: Chemistry 52, no. 1 (May 1990): 1–25. http://dx.doi.org/10.1016/1010-6030(90)87085-p.

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Kostyuk, N. N., T. A. Dik, and D. S. Umreiko. "Spectral properties and structure ofβ-diketonate metal complexes." Journal of Applied Spectroscopy 58, no. 1-2 (January 1993): 135–39. http://dx.doi.org/10.1007/bf00659174.

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Shen, Xiang, and Bing Yan. "A novel fluorescence probe for sensing organic amine vapors from a Eu3+β-diketonate functionalized bio-MOF-1 hybrid system." Journal of Materials Chemistry C 3, no. 27 (2015): 7038–44. http://dx.doi.org/10.1039/c5tc01287b.

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A classic anionic metal–organic framework (bio-MOF-1) for Eu3+-β-diketonate complex encapsulation has the utility of a sensory material for sensing volatile organic molecules, especially volatile amines.
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Dissertations / Theses on the topic "Metal diketonate"

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Lerach, Jordan O. "Investigations into the gas-phase rearrangements of some transition metal beta-diketonate complexes /." Connect to resource online, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1222114603.

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Lerach, Jordan O. "Investigations into the Gas-Phase Rearrangements of Some Transition Metal β-Diketonate Complexes." Youngstown State University / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1222114603.

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Kemats, Kyle. "Examining the Gas-Phase Fragmentation of Select Metal ß-diketonate Complexes Using Computational Methods." Youngstown State University / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1410787738.

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Fleming, Kathleen. "The Gas-Phase Ligand Exchange of Select Alkaline Earth and Transition Metal ß-diketonate Complexes." Youngstown State University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1465062889.

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Hunter, Gerald O. "The examination of the stability and reactivity of select transition metal [beta]-diketonate complexes during gas-phase ligand exchange reactions /." Connect to resource online, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1263671226.

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Lord, Rianne Michaela. "Synthesis of novel functionalised β-ketoiminate and β-diketonate metal complexes for their use in anti-cancer treatment." Thesis, University of Leeds, 2014. http://etheses.whiterose.ac.uk/6386/.

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This thesis is concerned with the synthesis, characterisation and evaluation of novel metal complexes for their application as anti-cancer agents. It contains the in vitro cell results, along with a range of other techniques to determine their biological relevance and their potential as anti-cancer agents. Chapter 1 contains an introduction to the project including a literature search, previously synthesised complexes and project aims Chapter 2 presents the synthesis and characterisation of novel β-diketonate and β-ketoiminate ligands. X-ray crystallographic data are analysed for some of the ligands. Chapter 3 discusses the synthesis and characterisation of novel β-ketoiminate ruthenium chloride complexes. X-ray crystallographic data are analysed for all of the complexes. Chapter 4 introduces the MTT technique for assessing cytotoxicity, and presents in vitro activities for the library of complexes synthesised in Chapter 3. Chapter 5 looks at modifications of the previous ruthenium (II) complexes, introducing new ligands and iridum metal centres. X-ray crystallographic data for all of these complexes has been discussed, along with in vitro activity against a range of cell lines. Chapter 6 introduces hypoxia and states the cytotoxicities of a range of complexes under 1.0% and 0.1% oxygen concentrations. Chapter 7 discusses mechanistic studies on the complexes, including hydrolysis, hydrophobicity, Comet assay, apoptosis and thioredoxin reductase inhibition. Chapter 8 introduces the previous group IV work within the group and an extension of the library by synthesis of β-ketoiminate titanium complexes. X-ray crystallographic analysis is discussed where applicable. Chapter 9 contains experimental details and characterisation data for all compounds described in Chapters 2, 3, 5 and 8. Also protocols for all the biological studies. Appendix presents a summary of X-ray crystallographic structure analysis for any crystals obtained within this work.
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Boulos, Victoria Marie. "The Gas-Phase Ligand Exchange of Select Metal Bis-diisopropylacetylacetonate Complexes." Youngstown State University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1503671099629922.

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Obi-Johnson, Bettie Jeanne. "Mechanistic analysis of the thermally induced decomposition of certain metal beta-diketonate precursors for chemical vapor deposition of electronic materials." Diss., Georgia Institute of Technology, 1999. http://hdl.handle.net/1853/30743.

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Hunter, Gerald Jr. "The Examination of the Stability and Reactivity of Select Transition Metal β-Diketonate Complexes during Gas-Phase Ligand Exchange Reactions." Youngstown State University / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1263671226.

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Gasior, James Kole. "The Gas-Phase Ligand Exchange of Trivalent Metal ß-Diketonates." Youngstown State University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1495099165708741.

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Books on the topic "Metal diketonate"

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Kessler, Vadim G. Metal beta-Diketonate Complexes: Chemistry and Applications. Wiley-VCH, 2007.

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I, Martynenko L., Vovna V. I, Dzi͡u︡benko N. G, Korotkikh O. A, Nauchnyĭ sovet po neorganicheskoĭ khimii (Akademii͡a︡ nauk SSSR), Moskovskiĭ gosudarstvennyĭ universitet im. M.V. Lomonosova., and Dalʹnevostochnyĭ gosudarstvennyĭ universitet (Vladivostok, Russia), eds. [Beta]-diketonaty metallov: Sbornik nauchnykh trudov. Vladivostok: Izd-vo Dalʹnevostochnogo universiteta, 1990.

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Book chapters on the topic "Metal diketonate"

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Stringer, Tameryn, and Rianne M. Lord. "Medicinal applications of early transition metal β-diketonato complexes." In Organometallic Chemistry, 92–109. Cambridge: Royal Society of Chemistry, 2022. http://dx.doi.org/10.1039/9781839167713-00092.

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Lockyer, Trevor N., and Raymond L. Martin. "Dithiolium Salts and Dithio-β-Diketone Complexes of the Transition Metals." In Progress in Inorganic Chemistry, 223–324. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470166284.ch4.

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Keppler, B. K., C. Friesen, H. G. Moritz, H. Vongerichten, and E. Vogel. "Tumor-inhibiting bis(β-Diketonato) metal complexes. Budotitane, cis-diethoxybis(1-phenylbutane-1,3-dionato)titanium(IV)." In Structure and Bonding, 97–127. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/3-540-54261-2_2.

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Ushida, Takahisa, Kazutoshi Higashiyama, and Izumi Hirabayashi. "Excimer Laser-Induced Chemical Vapor Deposition of Metal Oxides Thin Film from β-Diketone Complexes." In Advances in Superconductivity III, 981–84. Tokyo: Springer Japan, 1991. http://dx.doi.org/10.1007/978-4-431-68141-0_221.

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Zhang, Nan, Gai-feng Xue, Lei Zhang, Pu Liu, and Lina Wang. "Preparation of β-Diketone Modified Silica Gel and its Application to the Removal of Heavy Metal Ions from Industrial Wastewater." In T.T. Chen Honorary Symposium on Hydrometallurgy, Electrometallurgy and Materials Characterization, 565–71. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118364833.ch51.

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"__MPSCONT__2.2. aus Metall-Verbindungen und 1,3-Diketonat-Anionen." In En,X- und In,X-Verbindungen, edited by Heinz Kropf and Ernst Schaumann. Stuttgart: Georg Thieme Verlag, 1993. http://dx.doi.org/10.1055/b-0035-112126.

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Chand, K., Umesh, D. P. Dorairaj, and S. C. N. Hsu. "27.28 Product Class 28: β-Diketimines (1,3-Diimines)." In Knowledge Updates 2021/2. Stuttgart: Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/sos-sd-127-00466.

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Abstractβ-Diketimines, encountered frequently as “nacnac” ligands, have emerged as popular motifs among other ancillary supports. There has been a great deal of interest in these compounds as supporting ligands because of their strong binding to metal ions, their tunable steric and electronic effects, and their diversity in terms of bonding modes. A classical synthetic approach towards β-diketimines is direct condensation of pentane-2,4-diones (and 1,3-diketone analogues) with suitable amines in the presence of an acid source. Recent developments involve the use of molecular sieves to avoid purification problems and to improve yields. Herein, a thorough survey of the synthetic approaches to β-diketimine ligands and their metal complexes, and applications in coordination chemistry, has been compiled.
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Taber, Douglass F. "Metal-Mediated C–C Ring Construction: The Carreira Synthesis of (+)-Asperolide C." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0073.

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Djamaladdin G. Musaev and Huw M. L. Davies of Emory University effected (Chem. Sci. 2013, 4, 2844) enantioselective cyclopropanation of ethyl acrylate 2 with the α-diazo ester 1 to give 3 in high ee. Philippe Compain of the Université de Strasbourg used (J. Org. Chem. 2013, 78, 6751) SmI2 to cyclize 4 to the cyclobutanol 5. Jianrong (Steve) Zhou of Nanyang Technological University effected (Chem. Commun. 2013, 49, 11758) enantioselective Heck addition of 7 to the prochiral ester 6 to give the cyclopentene 8. Liu-Zhu Gong of USTC, Hefei added (Org. Lett. 2013, 15, 3958) the Rh enolate from the enantioselective ring expansion of the α-diazo ester 9 to the nitroalkene 10, to give 11 in high de. Stephen P. Fletcher of the University of Oxford set (Angew. Chem. Int. Ed. 2013, 52, 7995) the cyclic quaternary center of 14 by the enantioselective conjugate addition to 12 of the alkyl zirconocene derived from 13. Alexandre Alexakis of the University of Geneva reported (Chem. Eur. J. 2013, 19, 15226) high ee from the conjugate addition of alkenyl Al reagents (not illustrated) to 12. Paultheo von Zezschwitz of Philipps-Universität Marburg prepared (Adv. Synth. Catal. 2013, 355, 2651) the silyl enol ether 17 by trapping the intermediate from the conjugate addition of 16 to 15. Stefan Bräse of the Karlsruhe Institute of Technology effected (Eur. J. Org. Chem. 2013, 7110) conjugate addition to the prochiral dienone 18 to give the highly substi­tuted cyclohexenone 19. Ping Tian and Guo-Qiang Lin of the Shanghai Institute of Organic Chemistry cyclized (J. Am. Chem. Soc. 2013, 135, 11700) 20 to the kinetic, less stable epimer of the diketone 21. Rh-mediated intramolecular C–H insertion has been a powerful tool for the con­struction of cyclopentane derivatives. Douglass F. Taber of the University of Delaware found (J. Org. Chem. 2013, 78, 9772) that the Rh carbene derived from 22 was dis­criminating enough to target the more nucleophilic C–H bond, leading to the cyclohexanone 23. Kozo Shishido of the University of Tokushima observed (Org. Lett. 2013, 15, 3666) high diastereoselectivity in the intramolecular Heck cyclization of 24 to 25.
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Taber, Douglass F. "Metal-Mediated C–C Ring Construction: The Sun/Lin Synthesis of Huperzine A." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0074.

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Zachary T. Ball of Rice University found (Chem. Sci. 2014, 5, 1401) that the on-bead performance of a designed Rh- peptide complex was markedly superior to the corre­sponding solution catalysis for the addition of 2 to 1 to give 3. Jin-Quan Yu of Scripps/La Jolla achieved (J. Am. Chem. Soc. 2014, 136, 8138) remarkable ee in the conversion of 4 to 5. Adriaan J. Minnaard of the University of Groningen developed (Adv. Synth. Catal. 2014, 356, 2061) practical conditions for enantioselective conjugate addi­tion– enolate trapping, converting 6 to 8. Alexandre Alexakis of the University of Geneva had reported (Org. Lett. 2014, 16, 118) related results. Jérôme Waser of the Ecole Polytechnique Fédérale de Lausanne assembled (J. Am. Chem. Soc. 2014, 136, 6239) the amino cyclopentane 11 by adding 9 to 10. Jean-Luc Vasse of the Université de Reims used (Org. Lett. 2014, 16, 1506) the Schwartz reagent to cyclize 12 to 13. Eric V. Johnston and Armando Córdova of the University of Stockholm combined (Angew. Chem. Int. Ed. 2014, 53, 3447) Pd and organocatalysis in a cascade of first oxi­dation of 14, then conjugate addition by 15, then cyclization to 16. Professor Alexakis found (Org. Lett. 2014, 16, 2006) that the enolate from con­jugate addition to 17 could be trapped with a nitroalkene 18 to give, after in situ Nef reaction, the 1,4-diketone 19. Fangzhi Peng and Zhihui Shao of Yunnan University added (Chem. Eur. J. 2014, 20, 6112) malonate to the nitro alkene 20 to give an inter­mediate that could be carried to the cyclohexanone 21. Masahisa Nakada of Waseda University devised (Tetrahedron Lett. 2014, 55, 1100) a cascade conjugate reduc­tion—intramolecular conjugate addition to cyclize 22 to 23. Hye-Young Jang of Ajou University dimerized (Synthesis 2014, 46, 1329) cinnamaldehyde 24 with nitrometh­ane to give the fully-substituted cyclohexanol 25. In a remarkable cascade transformation, Joëlle Prunet of the University of Glasgow used (Org. Lett. 2014, 16, 3300) the Zhang Ru catalyst to cyclize 26 to the taxol skeleton 27. In an even more remarkable transformation, Professor Nakada showed (Tetrahedron Lett. 2014, 55, 1597) that cascade conjugate addition– conjugate addition converted 28 to 29, having the rare chair- boat- chair skeleton of the biologically potent fusidic acid and brasilicardin A.
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Taber, Douglass. "Synthesis of Heteroaromatics." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0066.

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Yasutaka Ishii of Kansai University has developed (J. Org. Chem. 2007, 72, 8820) a novel route to furans, using a mixed-metal catalyst to effect condensation of an aldehyde or 1,3 diketone such as 1 with an acceptor such as 2 to give the 3-furoate 3. In a complementary approach, Yong-Min Liang of Lanzhou University has found (J. Org. Chem. 2007, 72, 10276) that diazoacetate 5 will condense with an alkynyl ketone to give the 2-furoate 6. David W. Knight of Cardiff University has shown (Tetrahedron Lett. 2007, 48, 7709) that an alkynyl diol such as 7, readily available by dihydroxylation of the corrresponding alkenyl alkyne, cyclized to the furan on exposure to AgNO3 on silica gel. Professor Knight has also (Tetrahedron Lett. 2007, 48, 7906) established a route to poly-substituted pyrroles 10, by iodination of alkynyl sulfonamides such as 9. Similarly, Richard C. Larock of Iowa State University found (J. Org. Chem. 2007, 72, 9643) that I-Cl cyclized methoximes such as 11 to the corresponding iodo isoxazole 12, and Stephen L. Buchwald of MIT uncovered (Organic Lett. 2007, 9, 5521) the cyclization of an enamide such as 13 with I2 to the corresponding oxazole 14. In developing a more efficient route to a new class of materials that he has named “triazolamers”, Paramjit S. Arora of New York University was able (J. Org. Chem. 2007, 72, 7963) to effect diazo transfer to the amine 15 and subsequent condensation with 16 to give 17, without isolation of the intermediate azide. C. V. Asokan and E. R. Anabha of Mahatma Gandhi University have described (Tetrahedron Lett. 2007, 48, 5641) the activation of a ketone 18 followed by condensation with malononitrile 19 to give the pyridine 20. Hans-Ulrich Reissig of the Freie Universität Berlin has established (Organic Lett. 2007, 9, 5541) a complementary three-component coupling of a nitrile 21 with the allenyl anion 22, followed by a carboxylic acid 23 to deliver the pyridine 24. Akio Saito and Yuji Hanzawa of the Showa Pharmaceutical University have reported (Tetrahedron Lett. 2007, 48, 6852) the intramolecular Rh-catalyzed cyclization of a methoxime lactone such as 25 to the pyridine 26.
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Conference papers on the topic "Metal diketonate"

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Morris, J. B., and M. V. Johnston. "Multiphoton ioniztion of metal β-diketonates and metal tetraphenylporphyrin complexes: Ligand dissociation vs. molecular ionization." In AIP Conference Proceedings Volume 146. AIP, 1986. http://dx.doi.org/10.1063/1.35926.

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Ma, Dongzhe, Yiqun Wu, Xin Jiang, Zhimin Chen, and Xia Zuo. "Thermal and optical properties of rare earth metal β-Diketone Bipy complexes as optical recording materials." In Seventh International Symposium on Optical Storage (ISOS 2005), edited by Fuxi Gan and Lisong Hou. SPIE, 2005. http://dx.doi.org/10.1117/12.649798.

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