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Relevant bibliographies by topics / Organic syntheses

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Academic literature on the topic 'Organic syntheses'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 January 2023

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Journal articles on the topic "Organic syntheses"

1

Dai, Mingji, Xinpei Cai, and Yu Bai. "Total Syntheses of Spinosyn A." Synlett 29, no. 20 (2018): 2623–32. http://dx.doi.org/10.1055/s-0037-1610249.

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Spinosyn A is an important polycyclic natural product with impressive insecticidal activity and has been used worldwide in agriculture as the major component of Spinosad. Herein, four chemical total syntheses of spinosyn A are summarized. Its biosynthesis and a chemoenzymatic total synthesis are discussed as well.1 Biosynthesis2 The Evans Synthesis3 The Paquette Synthesis4 The Roush Synthesis5 The Liu Synthesis6 The Dai Synthesis7 Conclusions

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Huang, Jianhui, Caifeng Li, Liu Liu, and Xuegang Fu. "Norbornene in Organic Synthesis." Synthesis 50, no. 15 (2018): 2799–823. http://dx.doi.org/10.1055/s-0037-1610143.

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The norbornene skeleton possesses an alkene functionality with a fixed conformation, and represents unique reactivity. The use of norbornene and analogues as substrates is overviewed; reactivities are discussed as well as the role of norbornenes as ligands assisting modern organic transformations.1 Introduction2 Synthesis of Substituted Norbornenes2.1 Preparation of Functionalized Norbornenes by Deprotonation and Substitution Reactions2.2 Preparation of Functionalized Norbornenes under Palladium-Catalyzed Reaction Conditions2.3 Alkylation of Norbornene2.4 Multistep Synthesis3 Synthesis of Sub

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ZURER, PAMELA S. "OPTIMIZING ORGANIC SYNTHESES." Chemical & Engineering News 75, no. 18 (1997): 47–50. http://dx.doi.org/10.1021/cen-v075n018.p047.

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Ojima, Iwao. "New cyclization reactions in organic syntheses." Pure and Applied Chemistry 74, no. 1 (2002): 159–66. http://dx.doi.org/10.1351/pac200274010159.

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Recent development in the transition metal-catalyzed cyclization reactions for organic syntheses in the author's laboratories is summarized, which includes (i) novel silylcarbocyclizations (SiCaCs) and carbonylative carbotricyclizations, (ii) intramolecular silylformylations and desymmerization of siloxydiynes by sequential double silylformylation, (iii) efficient total synthesis of (+)-prosopinine, (iv) enantioselective desymmetrization of aminodienes, and (iv) new and efficient routes to 1-azabicyclo[x.y.0]alkane amino acids. All these processes are catalyzed by Rh or RhCo complexes, and us

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Fang, Zhang, and Yu Yang. "Research Progress of Application of Porous Polymer in Energy Storage." Advanced Materials Research 621 (December 2012): 27–30. http://dx.doi.org/10.4028/www.scientific.net/amr.621.27.

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Nowadays, one of the research emphases in clean energy field is to apply porous polymer as energy storage media to capture and save abundant energy. Researches in this area focus on theoretical methods and syntheses of new materials. Researches on theoretical methods include investigations on mechanical strength, characteristic of heat and mass transfer, internal structure and hydrophilicity of materials using mathematical, physical and chemical methods. Syntheses of new materials include synthesis of porous carbon and porous metal organic frameworks materials and construction of battery struc

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Lowe, Derek. "AI designs organic syntheses." Nature 555, no. 7698 (2018): 592–93. http://dx.doi.org/10.1038/d41586-018-03774-5.

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Scrivanti, A., G. Cavinato, L. Toniolo, and C. Botteghi. "Metals in organic syntheses." Journal of Organometallic Chemistry 286, no. 1 (1985): 115–20. http://dx.doi.org/10.1016/0022-328x(85)87240-5.

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Varma, Rajender S. "Solvent-free organic syntheses." Green Chemistry 1, no. 1 (1999): 43–55. http://dx.doi.org/10.1039/a808223e.

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Metzger, Jürgen O. "Solvent-Free Organic Syntheses." Angewandte Chemie International Edition 37, no. 21 (1998): 2975–78. http://dx.doi.org/10.1002/(sici)1521-3773(19981116)37:21<2975::aid-anie2975>3.0.co;2-a.

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Cavinato, G., L. Toniolo, and C. Botteghi. "Metals in organic syntheses." Journal of Molecular Catalysis 32, no. 2 (1985): 211–18. http://dx.doi.org/10.1016/0304-5102(85)80007-9.

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Dissertations / Theses on the topic "Organic syntheses"

1

Santangelo, Ellen M. "Stereoselective syntheses of semichemicals : Applications in ecological chemistry." Doctoral thesis, KTH, Chemistry, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-74.

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<p>This thesis describes the syntheses of semiochemicals and their applications in the development of control methods for pest insects. The compounds synthesized are divided into three groups: 1) Lepidoptera pheromones; 2) methyl substituted chiral pheromones and 3) aphid pheromones. </p><p>Different purification techniques have been explored in order to provide > 99% pure semiochemicals for field tests. Examples of the techniques are uses of urea inclusion complexes, argentum chromatography, low temperature crystallization and what we call the Baeckström isolation technique.</p><p>Iridoids ha

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Mercer, R. J. "Organic Transformations at metal centres." Thesis, University of Bristol, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.381446.

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Tan, Changqing. "Photochemical Silaylide, Silylene and Silene Syntheses." Thesis, University of North Texas, 1990. https://digital.library.unt.edu/ark:/67531/metadc501256/.

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The synthesis of o-(N,N-dimethylamino)methylphenyl tris (trimethylsilyl) silane (II), a photochemical precursor of o- (N,N-dimethylamino) methylphenyl (trimethylsilyl) sila ammonium ylide (intramolecular silylene complex) and otolyl(trimethylsilyl)silylene is reported. Photolysis of II at room temperature in a cyclohexane solution of triethyl silane produced the silylene ylide and the presumably uncomplexed isomer, a silylene, which is trapped to afford the 2-(o-(N,N-dimethylamino)methylphenyl) -1,1,1-triethyl 3,3,3-trimethyltrisilane, 33% yield. A second decomposition pathway, a photodeaminat

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Figuccia, Aude L. A. "Total asymmetric syntheses of iminosugars." Thesis, University of Oxford, 2015. http://ora.ox.ac.uk/objects/uuid:7075b45f-e3e1-4ae6-a544-4d6e54d4714e.

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This thesis is concerned with the development of ring-closing iodoamination and ringexpansion methodology and its subsequent application to the asymmetric syntheses of pyrrolidine and piperidine iminosugars. <strong>Chapter 1</strong> highlights the remarkable biological properties displayed by iminosugars and introduces methods for the formation of the pyrrolidine and piperidine sub-classes. <strong>Chapter 2</strong> describes investigations into the ring-closing iodoamination of bishomoallylic amines which occurs with concomitant <i>N</i>-debenzylation to give an iodomethyl pyrrolidine scaf

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O'Neill, Bridget. "Syntheses of novel 2-oxo esters : enzyme substrates designed for asymmetric synthesis." Thesis, University of Bristol, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.261316.

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Houlsby, Ian. "Asymmetric syntheses of polycyclic amines." Thesis, University of Oxford, 2017. https://ora.ox.ac.uk/objects/uuid:7c73384d-da09-41ee-b1fc-4509dd20aaf8.

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This thesis centers on the asymmetric synthesis of polycyclic amines, focussing on three distinct classes of polycyclic alkaloid natural products. The work aims to use common methodology of lithium amide conjugate additions as the source of asymmetry in all cases, and for each product class a single strategy is used to synthesise a variety compounds. Chapter 1 describes the importance of the synthesis of polycyclic alkaloids, highlighting three classes of compounds and documenting prior synthetic strategies. The classes discussed are: the Hancock alkaloids, hydroxymethyl-substituted azabicycle

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Shah, Rushabh Surendra. "Total syntheses of the nakinadine alkaloids." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:c022e538-9ff8-4914-8c17-dc0b3ed1fbae.

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This thesis is concerned with the development of methodology for the asymmetric syntheses of the nakinadine family of marine alkaloids and through these synthetic endeavours, seeks to confirm the structure and assign the relative and absolute configurations of these alkaloids for the first time.

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Bathgate, Antoinette. "Syntheses & reactions of azabicycles." Thesis, University of Leicester, 1988. http://hdl.handle.net/2381/33896.

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Several novel nitrogen containing bicyclic systems have been synthesised and their chemistry investigated. The kinetic and thermodynamic invertomer ratios of N-chloro-1,2,3,4-tetrahydro-2-keto-l, 4-iminonaphthalene derivatives were determined. The results suggested that a repulsive interaction existed between the positive end of the carbonyl dipole and the incoming electrophilic chlorine. Despite reaction under favourable solvolytic conditions, it appeared that homolysis of the N-chloroamines was favoured over heterolysis. Under conditions of negligible inversion, N-chloro-1,4-dihydro-1-methyl

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Chun, Doris Pik-Yiu. "Polyacene-based organic semiconductors syntheses, characterizations and applications in organic electronic devices /." Diss., Restricted to subscribing institutions, 2008. http://proquest.umi.com/pqdweb?did=1692370441&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.

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Hugo, Victor Ignatius. "Syntheses related to some naturally occurring naphthopyranquinones." Doctoral thesis, University of Cape Town, 1986. http://hdl.handle.net/11427/17036.

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Bibliography: pages 248-257.<br>The naphtho[2,3-c]pyran ring system occurs not infrequently in Nature as derivatives of the 5,10-quinone. Examples include the eleutherins, the nanaomycins and the protoaphins some of which have been shown to possess antibiotic activity. The synthesis of these natural products requires appropriate regiospecific aromatic oxygenation of 2- acetylnaphthoquinone. Syntheses of 3-acetyl-5-methoxy-1, 4- naphthoquinone and the corresponding 5,7-dimethoxy analogue are described and the use of these in the syntheses of several naturally occurring pyranquinones or their de

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Books on the topic "Organic syntheses"

1

1944-, Mulzer J., and Waldmann H, eds. Organic synthesis highlights. VCH, 1991.

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1957-, Czarnik Anthony W., ed. Solid-phase organic syntheses. John Wiley, 2001.

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Antineoplastic drugs: Organic syntheses. Wiley, 2015.

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P, Freeman Jeremiah, ed. Organic syntheses ...: Cumulative indices. John Wiley and Sons, 1995.

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Scott, Peter J. H., ed. Solid-Phase Organic Syntheses. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118336953.

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Czarnik, Anthony W., ed. Solid-Phase Organic Syntheses. John Wiley & Sons, Inc., 2001. http://dx.doi.org/10.1002/0471220434.

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Norman, R. O. C. Principles of organic synthesis. 3rd ed. ELBS with Chapman & Hall, 1993.

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1941-, Coxon J. M., ed. Principles of organic synthesis. 3rd ed. Blackie Academic & Professional, 1993.

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9

Bräse, Stefan. Organic azides: Syntheses and applications. John Wiley, 2010.

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Stefan, Bräse, and Banert Klaus, eds. Organic azides: Syntheses and applications. Wiley, 2009.

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Book chapters on the topic "Organic syntheses"

1

Carey, Francis A., and Richard J. Sundberg. "Multistep Syntheses." In Advanced Organic Chemistry. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-9797-7_13.

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Yoshida, Hisao. "Photocatalytic Organic Syntheses." In Nanostructure Science and Technology. Springer New York, 2010. http://dx.doi.org/10.1007/978-0-387-48444-0_27.

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Moeller, Therald. "Basic Beryllium Derivatives of Organic Acids." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132340.ch2.

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Wilke, G. "Organic Syntheses via Organometallics." In Organometallics in Organic Synthesis 2. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74269-9_1.

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Mukherjee, Sanjoy, and Bryan W. Boudouris. "Syntheses of Radical Polymers." In Organic Radical Polymers. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-58574-1_2.

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Kearney, Patrick C., Monica Fernandez, Mengmeng Fu, and John A. Flygare. "2-Aminothiazoles." In Solid-Phase Organic Syntheses. John Wiley & Sons, Inc., 2001. http://dx.doi.org/10.1002/0471220434.ch1.

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Fritch, Paul C., Adam M. Fivush, and Timothy M. Willson. "Preparation of Ameba Resin." In Solid-Phase Organic Syntheses. John Wiley & Sons, Inc., 2001. http://dx.doi.org/10.1002/0471220434.ch10.

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Smith, Adrian L., and Joseph G. Neduvelil. "An Efficient Solid-Phase Synthetic Route to 1,3-Disubstituted 2,4(1H,3H)-Quinazolinediones Suitable for Combinatorial Synthesis." In Solid-Phase Organic Syntheses. John Wiley & Sons, Inc., 2001. http://dx.doi.org/10.1002/0471220434.ch11.

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Alsina, Jordi, Knud J. Jensen, Michael F. Songster, Josef Vágner, Fernando Albericio, and George Barany. "Backbone Amide Linker (BAL) Strategy for Solid-Phase Synthesis." In Solid-Phase Organic Syntheses. John Wiley & Sons, Inc., 2001. http://dx.doi.org/10.1002/0471220434.ch12.

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Schuster, Matthias, and Siegfried Blechert. "The Allylsilyl Linker: Synthesis of Catalytic Binding of Alkenes and Alkynes to and Cleavage from Allyldimethylsilyl Polystyrene." In Solid-Phase Organic Syntheses. John Wiley & Sons, Inc., 2001. http://dx.doi.org/10.1002/0471220434.ch13.

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Conference papers on the topic "Organic syntheses"

1

Müller, Thomas, and Christa Kramer. "Syntheses of Functionalized Alkynylated Phenothiazines." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01856.

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Forni, J. A., A. F. P. Biajoli, E. T. da Penha, and C. R. D. Correia. "Expeditious syntheses of 3,4-dihydroisocoumarins and phthalides via a Heck-Matsuda reaction." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0044-1.

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Behramand, Fernando Molin, and Hugo Gallardo. "Syntheses and Photophysical Investigations of 2, 1, 3- benzoxadiazole based Luminescent Compounds." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0105-1.

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Pino-González, M., Noé Bernal, Raquel Casasola, and Inmaculada Robina. "Syntheses of new azepane derivatives from monosaccharides." In The 10th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2006. http://dx.doi.org/10.3390/ecsoc-10-01407.

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Stadlbauer, Wolfgang, Michaela Fischer, and Nathalie Lackner. "Syntheses and Reactions of Amino- and Azidophenalenones." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a014.

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Ullah, Hamid, Andre V. Ferreira, Manoel T. Rodrigues Jr та Fernando Coelho. "Syntheses of β-hydroxy-α-amino esters and non-proteinogenic α-amino acids from Morita-Baylis-Hillman adducts." У 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013819143637.

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Stadlbauer, Wolfgang, Georg Uray, and Guy Crépin Enoua. "4-Cyano-6-methoxyquinolones: Syntheses and Luminescence Properties." In The 13th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00171.

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Tiecco, M., L. Testaferri, C. Santi, et al. "Asymmetric Syntheses with a New Nitrogen Containing Chiral Diselenide." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01794.

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Perona, Almudena, Dionisia Sanza, Rosa Claramunta, and José Elguero. "Syntheses and Structural Studies of New Molecules Involving Hydrogen Bonds." In The 9th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01472.

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MAO, JIANG-GAO, CONG LEI, BING-PING YANG, JUN-LING SONG, and ABRAHAM CLEARFIELD. "SYNTHESES AND CRYSTAL STRUCTURES OF NOVEL INORGANIC-ORGANIC HYBRID MATERIALS." In Proceedings of the Seventh International Symposium on Hydrothermal Reactions. WORLD SCIENTIFIC, 2003. http://dx.doi.org/10.1142/9789812705228_0047.

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Reports on the topic "Organic syntheses"

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Reilly, S. D., D. R. Click, S. K. Grumbine, B. L. Scott, and J. G. Watkins. Asymmetric catalysis in organic synthesis. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/677032.

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Liu, Zhijian. Novel Aryne Chemistry in Organic Synthesis. Office of Scientific and Technical Information (OSTI), 2006. http://dx.doi.org/10.2172/897369.

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Bernstein, J., J. Y. Becker, S. Bittner, and S. S. Shaik. Electrically Conducting Organic Materials: Design, Synthesis and Characterization. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada195095.

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Folz, Katherine E. Synthesis and Characterization of Novel Organic Conducting Polymers. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada425003.

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Zhang, Honghu. Bioinspired synthesis and self-assembly of hybrid organic–inorganic nanomaterials. Office of Scientific and Technical Information (OSTI), 2016. http://dx.doi.org/10.2172/1409201.

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Ramírez, David A., Cecilia Silva-Díaz, Johan Ninanya, et al. Potato zero-tillage and mulching is promising in achieving agronomic gain in Asia. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.6.0072.

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Review question / Objective: The objective of this review is to analyze the effect of zero-tillage and organic mulching (with emphasis on rice-straw) on several Key Performance Indicators (KPIs) related to productivity, resources-use efficiency, and soil health, as well as, C footprint, and weed control for growing potatoes in rice-based systems in Asia. Can zero-tillage and organic mulching increase agronomic gain in potatoes crop in Asia? Rationale: Potato cultivation under zero-tillage and mulching (PZTM) between rice or rice-other crops projects a sustainable intensification of rice-based

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Sun, Ning. Process scale-up and optimization of the metal-organic framework synthesis. Office of Scientific and Technical Information (OSTI), 2020. http://dx.doi.org/10.2172/1618846.

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Matnishyan, Hakob A. Synthesis of New Organic Semiconducting Polymer Materials Having High Radiowave Absorption Rate. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada494519.

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Bao, Zhenan. Synthesis, Morphological and Electrical Characterization of Solution Processable Low Bandgap Organic Materials. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada494817.

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Morales, Alfredo Martin, Chris J. Rondeau, James Ross McElhanon, and Phillip James Cole. Synthesis of a photoresponsive polymer and its incorporation into an organic superlattice. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/921726.

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