Literatura científica selecionada sobre o tema "Organic Synthessis"
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Artigos de revistas sobre o assunto "Organic Synthessis"
Dai, Mingji, Xinpei Cai e Yu Bai. "Total Syntheses of Spinosyn A". Synlett 29, n.º 20 (7 de setembro de 2018): 2623–32. http://dx.doi.org/10.1055/s-0037-1610249.
Texto completo da fonteTrofimov, B. A., e 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 completo da fonteHuang, Jianhui, Caifeng Li, Liu Liu e Xuegang Fu. "Norbornene in Organic Synthesis". Synthesis 50, n.º 15 (25 de junho de 2018): 2799–823. http://dx.doi.org/10.1055/s-0037-1610143.
Texto completo da fonteTatrishvili, Tamara, e Omar Mukbaniani. "Cyclic Silicon Organic Copolymers: Synthesis and Investigation. Review". Chemistry & Chemical Technology 18, n.º 2 (14 de junho de 2024): 131–42. http://dx.doi.org/10.23939/chcht18.02.131.
Texto completo da fonteChabukswar, Vasant, Sanjay Bhavsar e 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 março de 2011): 37–40. http://dx.doi.org/10.23939/chcht05.01.037.
Texto completo da fonteFang, Zhang, e Yu Yang. "Research Progress of Application of Porous Polymer in Energy Storage". Advanced Materials Research 621 (dezembro de 2012): 27–30. http://dx.doi.org/10.4028/www.scientific.net/amr.621.27.
Texto completo da fonteYevchuk, Iryna, Oksana Demchyna, Viktoriya Kochubey, Hanna Romaniuk e Zenoviya Koval. "Synthesis and Characterization of Organic-Inorganic Membranes Containing Sulphogroups". Chemistry & Chemical Technology 7, n.º 1 (10 de março de 2013): 89–93. http://dx.doi.org/10.23939/chcht07.01.089.
Texto completo da fonteGarcía-Perulero, I., S. Murcia-Mascarós, J. Rubio e 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 dezembro de 2003): 389–96. http://dx.doi.org/10.3989/cyv.2003.v42.i6.627.
Texto completo da fonteSharma, Upendra, Inder Kumar e Rakesh Kumar. "Recent Advances in the Regioselective Synthesis of Indoles via C–H Activation/Functionalization". Synthesis 50, n.º 14 (28 de maio de 2018): 2655–77. http://dx.doi.org/10.1055/s-0037-1609733.
Texto completo da fonteWang, Yi, Han Ding e Ge Ging Xu. "Computer Aided Organic Synthesis Based on Graph Grammars". Applied Mechanics and Materials 411-414 (setembro de 2013): 227–30. http://dx.doi.org/10.4028/www.scientific.net/amm.411-414.227.
Texto completo da fonteTeses / dissertações sobre o assunto "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 completo da fonteInert 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 completo da fonteThe 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 completo da fonteAbnormal 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 completo da fonteQC 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 completo da fonteFyrner, 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 completo da fonteIn 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 completo da fonteCarbohydrates 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 completo da fonteBERTON, GIACOMO. "SYNTHESIS OF TRIPHENYLENES FOR SUPRAMOLECULAR APPLICATIONS". Doctoral thesis, Università degli Studi di Trieste, 2020. http://hdl.handle.net/11368/2969361.
Texto completo da fonteHagberg, 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 completo da fonteLivros sobre o assunto "Organic Synthessis"
Carruthers, W. Some modern methods of organic synthesis. 3a ed. Cambridge [Cambridgeshire]: Cambridge University Press, 1986.
Encontre o texto completo da fonte1944-, Mulzer J., e Waldmann H, eds. Organic synthesis highlights. Weinheim: VCH, 1991.
Encontre o texto completo da fonteHans-Günther, Schmalz, e Wirth Thomas 1964-, eds. Organic synthesis highlights V. Weinheim: Wiley-VCH, 2003.
Encontre o texto completo da fonteSmith, Michael. Organic synthesis. New York: McGraw-Hill, 1994.
Encontre o texto completo da fonteTaber, Douglass F. Organic Synthesis. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0470056312.
Texto completo da fonteMichael, Smith. Organic synthesis. 2a ed. Boston: McGraw-Hill, 2002.
Encontre o texto completo da fonteSmith, Michael B. Organic synthesis. New York: McGraw-Hill, 1994.
Encontre o texto completo da fonteWillis, Christine L. Organic synthesis. Oxford: Oxford University Press, 1995.
Encontre o texto completo da fonteVolke, J. Electrochemistry in organic synthesis. Berlin: Springer-Verlag, 1994.
Encontre o texto completo da fonteSmit, W. A. Organic synthesis: The science behind the art. Cambridge, UK: Royal Society of Chemistry, 1998.
Encontre o texto completo da fonteCapítulos de livros sobre o assunto "Organic Synthessis"
Yamada, Shinji. "Organic Synthesis". In The Cation–π Interaction, 95–143. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-7335-2_4.
Texto completo da fonteAmeta, Chetna, Arpit Kumar Pathak e P. B. Punjabi. "Organic Synthesis". In Sonochemistry, 45–113. Toronto : Apple Academic Press, 2018.: Apple Academic Press, 2018. http://dx.doi.org/10.1201/b22323-4.
Texto completo da fonteOkuyama, Tadashi, e Howard Maskill. "Organic Synthesis". In Organic Chemistry. Oxford University Press, 2013. http://dx.doi.org/10.1093/hesc/9780199693276.003.0023.
Texto completo da fonteWillis, Christine L., e Martin Wills. "Selected organic syntheses". In Organic Synthesis. Oxford University Press, 2022. http://dx.doi.org/10.1093/hesc/9780198557913.003.0008.
Texto completo da fonteMorrow, Gary W. "Brief Organic Review". In Bioorganic Synthesis. Oxford University Press, 2016. http://dx.doi.org/10.1093/oso/9780199860531.003.0004.
Texto completo da fonte"Alkyne Metathesis in Synthesis: Syntheses of (+)-Ferrugine and Anatoxin-α". In Organic Synthesis, 82–83. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0470056312.ch42.
Texto completo da fonteSmith, Michael B. "Retrosynthesis, Stereochemistry, and Conformations". In Organic Synthesis, 1–60. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-800720-4.00001-5.
Texto completo da fonteSmith, Michael B. "Acids, Bases, and Addition Reactions". In Organic Synthesis, 61–95. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-800720-4.00002-7.
Texto completo da fonteSmith, Michael B. "Functional Group Exchange Reactions". In Organic Synthesis, 97–160. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-800720-4.00003-9.
Texto completo da fonteSmith, Michael B. "Acids, Bases, and Functional Group Exchange Reactions". In Organic Synthesis, 161–83. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-800720-4.00004-0.
Texto completo da fonteTrabalhos de conferências sobre o assunto "Organic Synthessis"
Smith, Warren E., William J. Dallas, Heidi A. Schlitt e Walter Kullmann. "Reconstructing a Vector Current Distribution from its Magnetic Field Using Linear Estimation Theory". In Signal Recovery and Synthesis. Washington, D.C.: Optica Publishing Group, 1986. http://dx.doi.org/10.1364/srs.1986.wa2.
Texto completo da fonteBarbosa, Alexandre F., e Arlene G. Corrêa. "Synthesis of 9-substituted 9-deazaguanine derivatives". In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0125-2.
Texto completo da fonteAraujo, Yara J. K., Isac G. Rosset e André L. M. Porto. "A New Synthesis of Benzonitriles Catalyzed by Microwave Irradiation". In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0003-1.
Texto completo da fonteRosset, Isac G., e André L. M. Porto. "Transesterification and Quantification by 1H NMR of Triester Oleate by Candida antarctica Lipase". In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0004-1.
Texto completo da fonteda Silva, A. J. M., C. Schneider e V. Snieckus. "Construction of Polyarylated Fluorenones via chemoselective Ru- and Pd-Catalyzed Suzuki Cross-Coupling Reactions". In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0007-1.
Texto completo da fonteAndrighetto, Rosália, Helio G. Bonacorso, Jussara Navarini, Nícolas Krüger, Marcos A. P. Martins e Nilo Zanatta. "Highly Efficient Synthesis of CF3-Containing 7-Aminoquinolines From Cyclocondensation Reaction of Trifluoroacetyl Enamine Precursors". In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0008-1.
Texto completo da fonteAndrighetto, Rosália, Helio G. Bonacorso, Jussara Navarini, Nícolas Krüger, Marcos A. P. Martins e Nilo Zanatta. "General Pathway for One-Pot Synthesis of Trifluoromethyl- Containing 2-Amino-cycloalka[b][1,8]naphthyridines". In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0008-2.
Texto completo da fonteNavarini, Jussara, Helio G. Bonacorso, Carson W. Wiethan, Rosália Andrighetto, Fábio M. Luz, Marcos A. P. Martins e 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". In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0009-1.
Texto completo da fonteNavarini, Jussara, Helio G. Bonacorso, Carson W. Wiethan, Rosália Andrighetto, Marcos A. P. Martins e Nilo Zanatta. "Molecular Iodine - An Efficient Oxidative Reagent for Aromatization of Trifluoromethyl Substituted Chromenones". In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0009-2.
Texto completo da fonteRampon, Daniel S., Aloir A. Merlo e Paulo H. Schneider. "Synthesis of New Liquid-Crystalline Selenophenes via Electrophilic Cyclization of (Z)-Selenoenynes". In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0011-1.
Texto completo da fonteRelatórios de organizações sobre o assunto "Organic Synthessis"
Reilly, S. D., D. R. Click, S. K. Grumbine, B. L. Scott e J. G. Watkins. Asymmetric catalysis in organic synthesis. Office of Scientific and Technical Information (OSTI), novembro de 1998. http://dx.doi.org/10.2172/677032.
Texto completo da fonteRittman, Bruce. Biotic Transformations of Organic Contaminants. The Groundwater Project, 2023. http://dx.doi.org/10.21083/ousn4116.
Texto completo da fonteLiu, Zhijian. Novel Aryne Chemistry in Organic Synthesis. Office of Scientific and Technical Information (OSTI), dezembro de 2006. http://dx.doi.org/10.2172/897369.
Texto completo da fonteBernstein, J., J. Y. Becker, S. Bittner e S. S. Shaik. Electrically Conducting Organic Materials: Design, Synthesis and Characterization. Fort Belvoir, VA: Defense Technical Information Center, fevereiro de 1988. http://dx.doi.org/10.21236/ada195095.
Texto completo da fonteFolz, Katherine E. Synthesis and Characterization of Novel Organic Conducting Polymers. Fort Belvoir, VA: Defense Technical Information Center, maio de 2004. http://dx.doi.org/10.21236/ada425003.
Texto completo da fonteRamírez, David A., Cecilia Silva-Díaz, Johan Ninanya, Mariella Carbajal, Javier Rinza, Suresh K. Kakraliya, Marcel Gatto e 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, junho de 2022. http://dx.doi.org/10.37766/inplasy2022.6.0072.
Texto completo da fonteZhang, Honghu. Bioinspired synthesis and self-assembly of hybrid organic–inorganic nanomaterials. Office of Scientific and Technical Information (OSTI), dezembro de 2016. http://dx.doi.org/10.2172/1409201.
Texto completo da fonteSun, Ning. Process scale-up and optimization of the metal-organic framework synthesis. Office of Scientific and Technical Information (OSTI), maio de 2020. http://dx.doi.org/10.2172/1618846.
Texto completo da fonteSingh, Anjali. Amino Acids: Building Blocks of Proteins. ConductScience, junho de 2022. http://dx.doi.org/10.55157/cs20220612.
Texto completo da fonteMatnishyan, Hakob A. Synthesis of New Organic Semiconducting Polymer Materials Having High Radiowave Absorption Rate. Fort Belvoir, VA: Defense Technical Information Center, novembro de 2008. http://dx.doi.org/10.21236/ada494519.
Texto completo da fonte