Auswahl der wissenschaftlichen Literatur zum Thema „Organic Synthessis“
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Zeitschriftenartikel zum Thema "Organic Synthessis"
Dai, Mingji, Xinpei Cai und Yu Bai. „Total Syntheses of Spinosyn A“. Synlett 29, Nr. 20 (07.09.2018): 2623–32. http://dx.doi.org/10.1055/s-0037-1610249.
Der volle Inhalt der QuelleTrofimov, B. A., und E. Yu Schmidt. „SUPERBASES IN ORGANIC SYNTHESIS“. Chemical Problems 20, Nr. 4 (2022): 325–40. http://dx.doi.org/10.32737/2221-8688-2022-3-325-340.
Der volle Inhalt der QuelleHuang, Jianhui, Caifeng Li, Liu Liu und Xuegang Fu. „Norbornene in Organic Synthesis“. Synthesis 50, Nr. 15 (25.06.2018): 2799–823. http://dx.doi.org/10.1055/s-0037-1610143.
Der volle Inhalt der QuelleTatrishvili, Tamara, und Omar Mukbaniani. „Cyclic Silicon Organic Copolymers: Synthesis and Investigation. Review“. Chemistry & Chemical Technology 18, Nr. 2 (14.06.2024): 131–42. http://dx.doi.org/10.23939/chcht18.02.131.
Der volle Inhalt der QuelleChabukswar, Vasant, Sanjay Bhavsar und Amit Horne. „Organic Synthesis and Characterization of Electrically Conducting Poly(o-Toluidine) Doped with Organic Acid“. Chemistry & Chemical Technology 5, Nr. 1 (15.03.2011): 37–40. http://dx.doi.org/10.23939/chcht05.01.037.
Der volle Inhalt der QuelleFang, Zhang, und Yu Yang. „Research Progress of Application of Porous Polymer in Energy Storage“. Advanced Materials Research 621 (Dezember 2012): 27–30. http://dx.doi.org/10.4028/www.scientific.net/amr.621.27.
Der volle Inhalt der QuelleYevchuk, Iryna, Oksana Demchyna, Viktoriya Kochubey, Hanna Romaniuk und Zenoviya Koval. „Synthesis and Characterization of Organic-Inorganic Membranes Containing Sulphogroups“. Chemistry & Chemical Technology 7, Nr. 1 (10.03.2013): 89–93. http://dx.doi.org/10.23939/chcht07.01.089.
Der volle Inhalt der QuelleGarcía-Perulero, I., S. Murcia-Mascarós, J. Rubio und J. L. Oteo. „Síntesis y caracterización de materiales híbridos orgánico-inorgánicos de APS/PDMS“. Boletín de la Sociedad Española de Cerámica y Vidrio 42, Nr. 6 (30.12.2003): 389–96. http://dx.doi.org/10.3989/cyv.2003.v42.i6.627.
Der volle Inhalt der QuelleSharma, Upendra, Inder Kumar und Rakesh Kumar. „Recent Advances in the Regioselective Synthesis of Indoles via C–H Activation/Functionalization“. Synthesis 50, Nr. 14 (28.05.2018): 2655–77. http://dx.doi.org/10.1055/s-0037-1609733.
Der volle Inhalt der QuelleWang, Yi, Han Ding und Ge Ging Xu. „Computer Aided Organic Synthesis Based on Graph Grammars“. Applied Mechanics and Materials 411-414 (September 2013): 227–30. http://dx.doi.org/10.4028/www.scientific.net/amm.411-414.227.
Der volle Inhalt der QuelleDissertationen zum Thema "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.
Der volle Inhalt der QuelleInert 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.
Der volle Inhalt der QuelleThe 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.
Der volle Inhalt der QuelleAbnormal 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.
Der volle Inhalt der QuelleQC 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.
Der volle Inhalt der QuelleFyrner, 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.
Der volle Inhalt der QuelleIn 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.
Der volle Inhalt der QuelleCarbohydrates 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.
Der volle Inhalt der QuelleBERTON, GIACOMO. „SYNTHESIS OF TRIPHENYLENES FOR SUPRAMOLECULAR APPLICATIONS“. Doctoral thesis, Università degli Studi di Trieste, 2020. http://hdl.handle.net/11368/2969361.
Der volle Inhalt der QuelleHagberg, 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.
Der volle Inhalt der QuelleBücher zum Thema "Organic Synthessis"
Carruthers, W. Some modern methods of organic synthesis. 3. Aufl. Cambridge [Cambridgeshire]: Cambridge University Press, 1986.
Den vollen Inhalt der Quelle finden1944-, Mulzer J., und Waldmann H, Hrsg. Organic synthesis highlights. Weinheim: VCH, 1991.
Den vollen Inhalt der Quelle findenHans-Günther, Schmalz, und Wirth Thomas 1964-, Hrsg. Organic synthesis highlights V. Weinheim: Wiley-VCH, 2003.
Den vollen Inhalt der Quelle findenSmith, Michael. Organic synthesis. New York: McGraw-Hill, 1994.
Den vollen Inhalt der Quelle findenTaber, Douglass F. Organic Synthesis. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0470056312.
Der volle Inhalt der QuelleMichael, Smith. Organic synthesis. 2. Aufl. Boston: McGraw-Hill, 2002.
Den vollen Inhalt der Quelle findenSmith, Michael B. Organic synthesis. New York: McGraw-Hill, 1994.
Den vollen Inhalt der Quelle findenWillis, Christine L. Organic synthesis. Oxford: Oxford University Press, 1995.
Den vollen Inhalt der Quelle findenVolke, J. Electrochemistry in organic synthesis. Berlin: Springer-Verlag, 1994.
Den vollen Inhalt der Quelle findenSmit, W. A. Organic synthesis: The science behind the art. Cambridge, UK: Royal Society of Chemistry, 1998.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "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.
Der volle Inhalt der QuelleAmeta, Chetna, Arpit Kumar Pathak und 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.
Der volle Inhalt der QuelleOkuyama, Tadashi, und Howard Maskill. „Organic Synthesis“. In Organic Chemistry. Oxford University Press, 2013. http://dx.doi.org/10.1093/hesc/9780199693276.003.0023.
Der volle Inhalt der QuelleWillis, Christine L., und Martin Wills. „Selected organic syntheses“. In Organic Synthesis. Oxford University Press, 2022. http://dx.doi.org/10.1093/hesc/9780198557913.003.0008.
Der volle Inhalt der QuelleMorrow, Gary W. „Brief Organic Review“. In Bioorganic Synthesis. Oxford University Press, 2016. http://dx.doi.org/10.1093/oso/9780199860531.003.0004.
Der volle Inhalt der Quelle„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.
Der volle Inhalt der QuelleSmith, 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.
Der volle Inhalt der QuelleSmith, 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.
Der volle Inhalt der QuelleSmith, 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.
Der volle Inhalt der QuelleSmith, 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.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Organic Synthessis"
Smith, Warren E., William J. Dallas, Heidi A. Schlitt und 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.
Der volle Inhalt der QuelleBarbosa, Alexandre F., und 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.
Der volle Inhalt der QuelleAraujo, Yara J. K., Isac G. Rosset und 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.
Der volle Inhalt der QuelleRosset, Isac G., und 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.
Der volle Inhalt der Quelleda Silva, A. J. M., C. Schneider und 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.
Der volle Inhalt der QuelleAndrighetto, Rosália, Helio G. Bonacorso, Jussara Navarini, Nícolas Krüger, Marcos A. P. Martins und 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.
Der volle Inhalt der QuelleAndrighetto, Rosália, Helio G. Bonacorso, Jussara Navarini, Nícolas Krüger, Marcos A. P. Martins und 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.
Der volle Inhalt der QuelleNavarini, Jussara, Helio G. Bonacorso, Carson W. Wiethan, Rosália Andrighetto, Fábio M. Luz, Marcos A. P. Martins und 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.
Der volle Inhalt der QuelleNavarini, Jussara, Helio G. Bonacorso, Carson W. Wiethan, Rosália Andrighetto, Marcos A. P. Martins und 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.
Der volle Inhalt der QuelleRampon, Daniel S., Aloir A. Merlo und 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.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "Organic Synthessis"
Reilly, S. D., D. R. Click, S. K. Grumbine, B. L. Scott und J. G. Watkins. Asymmetric catalysis in organic synthesis. Office of Scientific and Technical Information (OSTI), November 1998. http://dx.doi.org/10.2172/677032.
Der volle Inhalt der QuelleRittman, Bruce. Biotic Transformations of Organic Contaminants. The Groundwater Project, 2023. http://dx.doi.org/10.21083/ousn4116.
Der volle Inhalt der QuelleLiu, Zhijian. Novel Aryne Chemistry in Organic Synthesis. Office of Scientific and Technical Information (OSTI), Dezember 2006. http://dx.doi.org/10.2172/897369.
Der volle Inhalt der QuelleBernstein, J., J. Y. Becker, S. Bittner und S. S. Shaik. Electrically Conducting Organic Materials: Design, Synthesis and Characterization. Fort Belvoir, VA: Defense Technical Information Center, Februar 1988. http://dx.doi.org/10.21236/ada195095.
Der volle Inhalt der QuelleFolz, Katherine E. Synthesis and Characterization of Novel Organic Conducting Polymers. Fort Belvoir, VA: Defense Technical Information Center, Mai 2004. http://dx.doi.org/10.21236/ada425003.
Der volle Inhalt der QuelleRamírez, David A., Cecilia Silva-Díaz, Johan Ninanya, Mariella Carbajal, Javier Rinza, Suresh K. Kakraliya, Marcel Gatto und 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, Juni 2022. http://dx.doi.org/10.37766/inplasy2022.6.0072.
Der volle Inhalt der QuelleZhang, Honghu. Bioinspired synthesis and self-assembly of hybrid organic–inorganic nanomaterials. Office of Scientific and Technical Information (OSTI), Dezember 2016. http://dx.doi.org/10.2172/1409201.
Der volle Inhalt der QuelleSun, Ning. Process scale-up and optimization of the metal-organic framework synthesis. Office of Scientific and Technical Information (OSTI), Mai 2020. http://dx.doi.org/10.2172/1618846.
Der volle Inhalt der QuelleSingh, Anjali. Amino Acids: Building Blocks of Proteins. ConductScience, Juni 2022. http://dx.doi.org/10.55157/cs20220612.
Der volle Inhalt der QuelleMatnishyan, Hakob A. Synthesis of New Organic Semiconducting Polymer Materials Having High Radiowave Absorption Rate. Fort Belvoir, VA: Defense Technical Information Center, November 2008. http://dx.doi.org/10.21236/ada494519.
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