Literatura académica sobre el tema "Organic Synthessis"
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Artículos de revistas sobre el tema "Organic Synthessis"
Dai, Mingji, Xinpei Cai y Yu Bai. "Total Syntheses of Spinosyn A". Synlett 29, n.º 20 (7 de septiembre de 2018): 2623–32. http://dx.doi.org/10.1055/s-0037-1610249.
Texto completoTrofimov, B. A. y E. Yu Schmidt. "SUPERBASES IN ORGANIC SYNTHESIS". Chemical Problems 20, n.º 4 (2022): 325–40. http://dx.doi.org/10.32737/2221-8688-2022-3-325-340.
Texto completoHuang, Jianhui, Caifeng Li, Liu Liu y Xuegang Fu. "Norbornene in Organic Synthesis". Synthesis 50, n.º 15 (25 de junio de 2018): 2799–823. http://dx.doi.org/10.1055/s-0037-1610143.
Texto completoTatrishvili, Tamara y Omar Mukbaniani. "Cyclic Silicon Organic Copolymers: Synthesis and Investigation. Review". Chemistry & Chemical Technology 18, n.º 2 (14 de junio de 2024): 131–42. http://dx.doi.org/10.23939/chcht18.02.131.
Texto completoChabukswar, Vasant, Sanjay Bhavsar y Amit Horne. "Organic Synthesis and Characterization of Electrically Conducting Poly(o-Toluidine) Doped with Organic Acid". Chemistry & Chemical Technology 5, n.º 1 (15 de marzo de 2011): 37–40. http://dx.doi.org/10.23939/chcht05.01.037.
Texto completoFang, Zhang y Yu Yang. "Research Progress of Application of Porous Polymer in Energy Storage". Advanced Materials Research 621 (diciembre de 2012): 27–30. http://dx.doi.org/10.4028/www.scientific.net/amr.621.27.
Texto completoYevchuk, Iryna, Oksana Demchyna, Viktoriya Kochubey, Hanna Romaniuk y Zenoviya Koval. "Synthesis and Characterization of Organic-Inorganic Membranes Containing Sulphogroups". Chemistry & Chemical Technology 7, n.º 1 (10 de marzo de 2013): 89–93. http://dx.doi.org/10.23939/chcht07.01.089.
Texto completoGarcía-Perulero, I., S. Murcia-Mascarós, J. Rubio y J. L. Oteo. "Síntesis y caracterización de materiales híbridos orgánico-inorgánicos de APS/PDMS". Boletín de la Sociedad Española de Cerámica y Vidrio 42, n.º 6 (30 de diciembre de 2003): 389–96. http://dx.doi.org/10.3989/cyv.2003.v42.i6.627.
Texto completoSharma, Upendra, Inder Kumar y Rakesh Kumar. "Recent Advances in the Regioselective Synthesis of Indoles via C–H Activation/Functionalization". Synthesis 50, n.º 14 (28 de mayo de 2018): 2655–77. http://dx.doi.org/10.1055/s-0037-1609733.
Texto completoWang, Yi, Han Ding y Ge Ging Xu. "Computer Aided Organic Synthesis Based on Graph Grammars". Applied Mechanics and Materials 411-414 (septiembre de 2013): 227–30. http://dx.doi.org/10.4028/www.scientific.net/amm.411-414.227.
Texto completoTesis sobre el tema "Organic Synthessis"
Paradis, Michel 1976. "The design and synthessis of platinum-based DNA intercalators /". Thesis, McGill University, 2000. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=31523.
Texto completoInert and stable transition-metal complexes are already being used for this purpose. Square planar platinum (II) complexes containing an aromatic heterocyclic ligand can insert and stack between the double helix base pairs. Two known ligands, DPPZ and phi, do intercalate DNA when chelating ruthenium, rhodium, or osmium.
Here are presented the syntheses of [Pt(NH3)2DPPZ](CF 3SO3)2, [Pt(en)DPPZ](CF3SO3) 2, [Pt(phen)DPPZ](CF3SO3)2, [Pt(Me 2bpy)DPPZ](CF3SO3)2, and [Pt(phendione)DPPZ](CF 3SO3)2, and the attempted syntheses of [Pt(en)phi](PF 6)2 and [Pt(phen)phi](PF6)2. The binding constants of [Pt(NH3)2DPPZ](CF3SO3) 2 and [Pt(en)DPPZ](CF3SO3)2 to calf thymus DNA have been determined. The knowledge coming from the synthetic strategy to obtain monomers has allowed the synthesis of a platinum-based dimer, [(DPPZ)Pt{DPPZ(11-11 ')DPPZ}Pt(DPPZ)](CF3SO3)4, having two intercalative DPPZ ends. We hope that this bis-intercalator will bring into close proximity two DNA strands.
Phung, Bich Tuyen. "Etude de la sélectivité dans la réaction de Buchner". Electronic Thesis or Diss., Université Grenoble Alpes, 2024. https://theses.hal.science/tel-04651531.
Texto completoThe work presented in this manuscript is divided into two main parts. Firstly, a study about the problem of chemoselectivity during the intramolecular carbene transfer reaction will be presented. The diazo compound bearing different substituent was synthesized as precursor of carbene, and then the carbene transfer reaction was performed in the presence of the Rh2(OAc)4 catalyst. The result displayed the competition between Buchner reaction and C‒H insertion reaction at benzylic position, depended on the substituent. DFT calculations were subsequently conducted to complete the information obtained experimentally. The second major focus of this manuscript involves exploring the reactivity of N-sulfonyl-1,2,3-triazole. N-sulfonyl-1,2,3-triazole precursors were generated using the CuAAC method. The intermolecular formal [3+2] cycloaddition reaction with aromatics catalysed by chiral Rh(II) was then studied
Trupina, Snjezana. "Synthesis of Metalloporphyrins with Oligothiophenes as Probes for Amyloid Diseases". Thesis, Linköping University, Linköping University, Organic Chemistry, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-57989.
Texto completoAbnormal aggregation of misfolded proteins is related to numerous neurodegenerative diseases, which include Alzheimer’s, Parkinson’s disease and prion diseases. Luminescent conjugated probes (LCPs) have been used as dyes for these supramolecular assemblies termed amyloid fibrils. To these probes, metalloporphyrin (MP) derivates have been attached to achieve new spectroscopic properties, which will allow for new ways to study protein aggregation diseases.
In this thesis the synthesis of two different LCPs anchored porphyrin derivates are described. The LCPs are synthesized from 3-thiopheneacetic acid and additional thiophene units are added with the use of Suzuki cross coupling reaction. The porphyrin is synthesized from pyrrol, benzaldehyde and methyl-4- formylbenzoate in a condensation reaction. In the first target molecule (TM) the porphyrin and thiophene are coupled with a spacer and the second one is a direct coupling between the two compounds.
Tilliet, Mélanie. "Synthesis and study of new oxazoline-based ligands". Doctoral thesis, KTH, Organisk kemi, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4858.
Texto completoQC 20100914
Winberg, Karl Johan. "Carborane Derivatives for Nuclide Therapy and Imaging : Synthesis and Radio-labelling". Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ-bibl. [distributör], 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3561.
Texto completoFyrner, Timmy. "Synthesis of Structures Related to Antifreeze Glycoproteins". Thesis, Linköping University, The Department of Physics, Chemistry and Biology, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-11941.
Texto completoIn this thesis, synthesis of structures related to antifreeze glycoproteins (AFGPs) are presented. Synthetic routes to a protected carbohydrate derivative, 2,3,4,6-tetra-O-benzyl-β-galactopyranosyl-(1→3)-2-deoxy-2-azido-4,6-di-O-benzyl-β-D-thio-1-galactopyranoside, and a tBu-Ala-Thr-Ala-Fmoc tripeptide, are described. These compounds are meant to be used in the assembly of AFGPs and analogues thereof. A Gal-GlcN disaccharide was synthesized via glycosylation between the donor, bromo-2-O-benzoyl-3,4,6-tri-O-benzyl-α-Dgalactopyranoside, and acceptor, ethyl 4,6-O-benzylidene-2-deoxy-2-N-phthalimido-β-D-1-thio-glucopyranoside, using silver triflate activation. Subsequent epimerization to a Gal-GalN disaccharide was achieved using Moffatt oxidation followed by L-selectride® reduction. The tripeptide was synthesized in a short and convenient manner using solid phase peptide synthesis with immobilized Fmoc-Ala on Wang® resins as starting point.
Larsson, Andreas. "Synthesis, structure and conformation of oligo- and polysaccharides". Doctoral thesis, Stockholm University, Department of Organic Chemistry, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-172.
Texto completoCarbohydrates are a complex group of biomolecules with a high structural diversity. Their almost omnipresent occurrence has generated a broad field of research in both biology and chemistry. This thesis focuses on three different aspects of carbohydrate chemistry, synthesis, structure elucidation and the conformational analysis of carbohydrates.
The first paper describes the synthesis of a penta- and a tetrasaccharide related to the highly branched capsular polysaccharide from Streptococcus pneumoniae type 37. In the second paper, the structure of the O-antigenic repeating unit from the lipopolysaccharide of E. coli 396/C1 was determined along with indications of the structure of the biological repeating unit. In addition, its structural and immunological relationship with E. coli O126 is discussed. In the third paper, partially protected galactopyranosides were examined to clarify the origin of an intriguing 4JHO,H coupling, where a W-mediated coupling pathway was found to operate. In the fourth paper, the conformation of methyl a-cellobioside is studied with a combination of molecular dynamics simulations and NMR spectroscopy. In addition to the expected syn-conformation, detection and quantification of anti-ø and anti-ψ conformers was also possible.
Esfandiarfard, Keyhan. "Novel Organophosphorus Compounds for Materials and Organic Synthesis". Doctoral thesis, Uppsala universitet, Molekylär biomimetik, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-328295.
Texto completoBERTON, GIACOMO. "SYNTHESIS OF TRIPHENYLENES FOR SUPRAMOLECULAR APPLICATIONS". Doctoral thesis, Università degli Studi di Trieste, 2020. http://hdl.handle.net/11368/2969361.
Texto completoHagberg, Daniel. "Synthesis of Organic Chromophores for Dye Sensitized Solar Cells". Licentiate thesis, Stockholm : Kemi, Kungliga Tekniska högskolan, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4600.
Texto completoLibros sobre el tema "Organic Synthessis"
Carruthers, W. Some modern methods of organic synthesis. 3a ed. Cambridge [Cambridgeshire]: Cambridge University Press, 1986.
Buscar texto completo1944-, Mulzer J. y Waldmann H, eds. Organic synthesis highlights. Weinheim: VCH, 1991.
Buscar texto completoHans-Günther, Schmalz y Wirth Thomas 1964-, eds. Organic synthesis highlights V. Weinheim: Wiley-VCH, 2003.
Buscar texto completoSmith, Michael. Organic synthesis. New York: McGraw-Hill, 1994.
Buscar texto completoTaber, Douglass F. Organic Synthesis. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0470056312.
Texto completoMichael, Smith. Organic synthesis. 2a ed. Boston: McGraw-Hill, 2002.
Buscar texto completoSmith, Michael B. Organic synthesis. New York: McGraw-Hill, 1994.
Buscar texto completoWillis, Christine L. Organic synthesis. Oxford: Oxford University Press, 1995.
Buscar texto completoVolke, J. Electrochemistry in organic synthesis. Berlin: Springer-Verlag, 1994.
Buscar texto completoSmit, W. A. Organic synthesis: The science behind the art. Cambridge, UK: Royal Society of Chemistry, 1998.
Buscar texto completoCapítulos de libros sobre el tema "Organic Synthessis"
Yamada, Shinji. "Organic Synthesis". En The Cation–π Interaction, 95–143. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-7335-2_4.
Texto completoAmeta, Chetna, Arpit Kumar Pathak y P. B. Punjabi. "Organic Synthesis". En Sonochemistry, 45–113. Toronto : Apple Academic Press, 2018.: Apple Academic Press, 2018. http://dx.doi.org/10.1201/b22323-4.
Texto completoOkuyama, Tadashi y Howard Maskill. "Organic Synthesis". En Organic Chemistry. Oxford University Press, 2013. http://dx.doi.org/10.1093/hesc/9780199693276.003.0023.
Texto completoWillis, Christine L. y Martin Wills. "Selected organic syntheses". En Organic Synthesis. Oxford University Press, 2022. http://dx.doi.org/10.1093/hesc/9780198557913.003.0008.
Texto completoMorrow, Gary W. "Brief Organic Review". En Bioorganic Synthesis. Oxford University Press, 2016. http://dx.doi.org/10.1093/oso/9780199860531.003.0004.
Texto completo"Alkyne Metathesis in Synthesis: Syntheses of (+)-Ferrugine and Anatoxin-α". En Organic Synthesis, 82–83. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0470056312.ch42.
Texto completoSmith, Michael B. "Retrosynthesis, Stereochemistry, and Conformations". En Organic Synthesis, 1–60. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-800720-4.00001-5.
Texto completoSmith, Michael B. "Acids, Bases, and Addition Reactions". En Organic Synthesis, 61–95. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-800720-4.00002-7.
Texto completoSmith, Michael B. "Functional Group Exchange Reactions". En Organic Synthesis, 97–160. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-800720-4.00003-9.
Texto completoSmith, Michael B. "Acids, Bases, and Functional Group Exchange Reactions". En Organic Synthesis, 161–83. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-800720-4.00004-0.
Texto completoActas de conferencias sobre el tema "Organic Synthessis"
Smith, Warren E., William J. Dallas, Heidi A. Schlitt y Walter Kullmann. "Reconstructing a Vector Current Distribution from its Magnetic Field Using Linear Estimation Theory". En Signal Recovery and Synthesis. Washington, D.C.: Optica Publishing Group, 1986. http://dx.doi.org/10.1364/srs.1986.wa2.
Texto completoBarbosa, Alexandre F. y Arlene G. Corrêa. "Synthesis of 9-substituted 9-deazaguanine derivatives". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0125-2.
Texto completoAraujo, Yara J. K., Isac G. Rosset y André L. M. Porto. "A New Synthesis of Benzonitriles Catalyzed by Microwave Irradiation". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0003-1.
Texto completoRosset, Isac G. y André L. M. Porto. "Transesterification and Quantification by 1H NMR of Triester Oleate by Candida antarctica Lipase". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0004-1.
Texto completoda Silva, A. J. M., C. Schneider y V. Snieckus. "Construction of Polyarylated Fluorenones via chemoselective Ru- and Pd-Catalyzed Suzuki Cross-Coupling Reactions". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0007-1.
Texto completoAndrighetto, Rosália, Helio G. Bonacorso, Jussara Navarini, Nícolas Krüger, Marcos A. P. Martins y Nilo Zanatta. "Highly Efficient Synthesis of CF3-Containing 7-Aminoquinolines From Cyclocondensation Reaction of Trifluoroacetyl Enamine Precursors". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0008-1.
Texto completoAndrighetto, Rosália, Helio G. Bonacorso, Jussara Navarini, Nícolas Krüger, Marcos A. P. Martins y Nilo Zanatta. "General Pathway for One-Pot Synthesis of Trifluoromethyl- Containing 2-Amino-cycloalka[b][1,8]naphthyridines". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0008-2.
Texto completoNavarini, Jussara, Helio G. Bonacorso, Carson W. Wiethan, Rosália Andrighetto, Fábio M. Luz, Marcos A. P. Martins y Nilo Zanatta. "Synthesis of New 5-Trifluoromethyl-3-alkyl[aryl(heteroaryl)]-4- (2-benzyl-3-hydroxycyclohex-2-enone-2-yl)-1H-pyrazoles by a Ring-Opening Reaction". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0009-1.
Texto completoNavarini, Jussara, Helio G. Bonacorso, Carson W. Wiethan, Rosália Andrighetto, Marcos A. P. Martins y Nilo Zanatta. "Molecular Iodine - An Efficient Oxidative Reagent for Aromatization of Trifluoromethyl Substituted Chromenones". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0009-2.
Texto completoRampon, Daniel S., Aloir A. Merlo y Paulo H. Schneider. "Synthesis of New Liquid-Crystalline Selenophenes via Electrophilic Cyclization of (Z)-Selenoenynes". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0011-1.
Texto completoInformes sobre el tema "Organic Synthessis"
Reilly, S. D., D. R. Click, S. K. Grumbine, B. L. Scott y J. G. Watkins. Asymmetric catalysis in organic synthesis. Office of Scientific and Technical Information (OSTI), noviembre de 1998. http://dx.doi.org/10.2172/677032.
Texto completoRittman, Bruce. Biotic Transformations of Organic Contaminants. The Groundwater Project, 2023. http://dx.doi.org/10.21083/ousn4116.
Texto completoLiu, Zhijian. Novel Aryne Chemistry in Organic Synthesis. Office of Scientific and Technical Information (OSTI), diciembre de 2006. http://dx.doi.org/10.2172/897369.
Texto completoBernstein, J., J. Y. Becker, S. Bittner y S. S. Shaik. Electrically Conducting Organic Materials: Design, Synthesis and Characterization. Fort Belvoir, VA: Defense Technical Information Center, febrero de 1988. http://dx.doi.org/10.21236/ada195095.
Texto completoFolz, Katherine E. Synthesis and Characterization of Novel Organic Conducting Polymers. Fort Belvoir, VA: Defense Technical Information Center, mayo de 2004. http://dx.doi.org/10.21236/ada425003.
Texto completoRamírez, David A., Cecilia Silva-Díaz, Johan Ninanya, Mariella Carbajal, Javier Rinza, Suresh K. Kakraliya, Marcel Gatto y Jan Kreuze. Potato zero-tillage and mulching is promising in achieving agronomic gain in Asia. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, junio de 2022. http://dx.doi.org/10.37766/inplasy2022.6.0072.
Texto completoZhang, Honghu. Bioinspired synthesis and self-assembly of hybrid organic–inorganic nanomaterials. Office of Scientific and Technical Information (OSTI), diciembre de 2016. http://dx.doi.org/10.2172/1409201.
Texto completoSun, Ning. Process scale-up and optimization of the metal-organic framework synthesis. Office of Scientific and Technical Information (OSTI), mayo de 2020. http://dx.doi.org/10.2172/1618846.
Texto completoSingh, Anjali. Amino Acids: Building Blocks of Proteins. ConductScience, junio de 2022. http://dx.doi.org/10.55157/cs20220612.
Texto completoMatnishyan, Hakob A. Synthesis of New Organic Semiconducting Polymer Materials Having High Radiowave Absorption Rate. Fort Belvoir, VA: Defense Technical Information Center, noviembre de 2008. http://dx.doi.org/10.21236/ada494519.
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