Auswahl der wissenschaftlichen Literatur zum Thema „Diels-Alder cycloaddition reactions“
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Zeitschriftenartikel zum Thema "Diels-Alder cycloaddition reactions"
Grygorenko, Oleksandr O., Viktoriia S. Moskvina, Oleksandr V. Hryshchuk und Andriy V. Tymtsunik. „Cycloadditions of Alkenylboronic Derivatives“. Synthesis 52, Nr. 19 (24.06.2020): 2761–80. http://dx.doi.org/10.1055/s-0040-1707159.
Der volle Inhalt der QuelleBurnell, D. Jean, und Zdenek Valenta. „π-Facial stereoselectivity in the Diels–Alder reactions of a rigid carbocyclic diene: spiro(bicyclo[2.2.1]heptane-2,1′-[2,4]cyclopentadiene)“. Canadian Journal of Chemistry 69, Nr. 1 (01.01.1991): 179–84. http://dx.doi.org/10.1139/v91-028.
Der volle Inhalt der QuelleSoares, Maria I. L., Ana L. Cardoso und Teresa M. V. D. Pinho e Melo. „Diels–Alder Cycloaddition Reactions in Sustainable Media“. Molecules 27, Nr. 4 (15.02.2022): 1304. http://dx.doi.org/10.3390/molecules27041304.
Der volle Inhalt der QuelleZhou, You-Yun, und Christopher Uyeda. „Catalytic reductive [4 + 1]-cycloadditions of vinylidenes and dienes“. Science 363, Nr. 6429 (21.02.2019): 857–62. http://dx.doi.org/10.1126/science.aau0364.
Der volle Inhalt der QuelleZezula, Josef, Tomáš Hudlický und Ion Ghiviriga. „Intramolecular Diels-Alder Cycloadditions of cis-Cyclohexadienediols Derived Enzymatically from (2-Azidoethyl)benzene. Construction of Highly Functionalized Bridged Isoquinoline Synthons“. Collection of Czechoslovak Chemical Communications 66, Nr. 8 (2001): 1269–86. http://dx.doi.org/10.1135/cccc20011269.
Der volle Inhalt der QuellePratt, Andrew J., Phillip M. Rendle und Peter J. Steel. „Anticancer Prodrug Studies: Diels - Alder Chemistry of 1-Methylthio-1-(p-tolylsulfonyl)ethene“. Australian Journal of Chemistry 64, Nr. 7 (2011): 945. http://dx.doi.org/10.1071/ch10450.
Der volle Inhalt der QuelleCarlini, Rina, Kerianne Higgs, Nicholas Taylor und Russell Rodrigo. „Diels–Alder adducts of ortho-benzoquinones: rearrangements and further transformations“. Canadian Journal of Chemistry 75, Nr. 6 (01.06.1997): 805–16. http://dx.doi.org/10.1139/v97-097.
Der volle Inhalt der QuelleAyadi, Sameh, und Manef Abderrabba. „Étude DFT des réactions de cycloaddition de type Diels–Alder sur le 4-aza-6-nitrobenzofuroxane“. Canadian Journal of Chemistry 85, Nr. 5 (01.05.2007): 331–35. http://dx.doi.org/10.1139/v07-026.
Der volle Inhalt der QuellePiers, Edward, Richard W. Friesen, Paul Kao, Steven J. Rettig und James Trotter. „Synthesis of functionalized hexahydro-, octahydro-, and decahydro-1H-phenalenes via Diels–Alder reactions of 1-methylene-4a-methoxycarbonyl-1,2,3,4,4a,5,6,7-octahydronaphthalene and related dienes“. Canadian Journal of Chemistry 71, Nr. 9 (01.09.1993): 1463–83. http://dx.doi.org/10.1139/v93-188.
Der volle Inhalt der QuelleKotha, Sambasivarao, Milind Meshram und Nageswara Panguluri. „Advanced Approaches to Post-Assembly Modification of Peptides by Transition-Metal-Catalyzed Reactions“. Synthesis 51, Nr. 09 (25.03.2019): 1913–22. http://dx.doi.org/10.1055/s-0037-1612418.
Der volle Inhalt der QuelleDissertationen zum Thema "Diels-Alder cycloaddition reactions"
Chumachenko, Natasha. „[Beta]-acryloyloxysulfonyl tethers for intramolecular Diels-Alder cycloaddition reactions“. [Kent, Ohio] : Kent State University, 2005. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=kent1135392557.
Der volle Inhalt der QuelleTitle from PDF t.p. (viewed July 28, 2005). Author's first name appears on the abstract page as: Nataliya. Advisor: Paul Sampson. Keywords: b-hydroxysulfones; [beta]-hydroxysulfones; epoxide opening; intramolecular Diels-Alder reaction; vinylsulfones. Includes bibliographical references (p.194- 202).
Chumachenko, Nataliya. „b-Acryloyloxysulfonyl Tethers for Intramolecular Diels-Alder Cycloaddition Reactions“. Kent State University / OhioLINK, 2005. http://rave.ohiolink.edu/etdc/view?acc_num=kent1135392557.
Der volle Inhalt der QuelleShengxian, Zhao. „Cycloaddition reactions of meso-tetraarylporphyrins“. Doctoral thesis, Universidade de Aveiro, 2005. http://hdl.handle.net/10773/4871.
Der volle Inhalt der QuelleO trabalho apresentado nesta dissertação descreve o comportamento de meso-tetra-arilporfirinas em reacções de ciclo-adição e suas possíveis aplicações na síntese de novas porfirinas com grupos policíclicos aromáticos (“π-extended porphyrins”). No capítulo 1 apresenta-se uma revisão das aplicações de porfirinas e compostos afins e também das reacções de ciclo-adição que envolvem ligações duplas (periféricas) do macrociclo. O capítulo 2 descreve o trabalho feito em reacções de cicloadição 1,3-dipolar de meso-tetra-arilporfirinas com iletos de azometino. Considerou-se primeiramente a reactividade de meso-tetra-arilporfirinas simétricas perante iletos de azometino. Em seguida estudaram-se as reacções de meso-tetra-arilporfirinas de tipo A3B também com iletos de azometino. Seguidamente consideraram-se estudos similares mas desta vez visando reacções de cicloadição 1,3-dipolar, intramolecular, com meso-(o-formilfenil)porfirinas. O capítulo 3 descreve os estudos efectuados sobre transformações de Diels-Alder de meso-tetra-arilporfirinas com orto-quinodimetano de tipo pirazínico. Os novos produtos (“π-extended porphyrins”) obtiveram-se por ciclização intramolecular entre grupos meso-arilo e o anel quinoxalínico fundido em β. No capítulo 4 descrevem-se os estudos de ciclo-adição 1,3-dipolar de iletos N-piridínicos contendo o macrociclo porfirínico. As reacções de tais iletos com quinonas e com acetilenodicarboxilato de dimetilo originaram porfirinas subsituidas em posição meso com grupos de tipo indolizina. Essas quinonas foram usadas em excesso, actuando como dipolarófilos iniciais e depois como oxidantes. Obtiveram-se novos compostos aromáticos policíclicos nas reacções daqueles iletos com alcenos electronicamente deficientes e na ausência de oxidante. O capítulo 5 relata os resultados dos estudos de síntese de porfirinas com grupos policíclicos aromáticos através de reacções electrocíclicas. Isso foi conseguido a partir das reacções de porfirinas contendo grupos cetónicos com iletos de fósforo. A caracterização estrutural destes novos derivados fez-se recorrendo ao uso de técnicas espectroscópicas modernas, especialmente através de estudos de RMN. Estes métodos de RMN incluíram métodos mono e bidimensionais (1D: 1H, 13C, DEPT; 2D: COSY, NOESY, HSQC, HMBC).
The work presented in this dissertation describes the cycloaddition reaction studies concerning meso-tetraarylporphyrins and also their applications in the synthesis of novel π-extended porphyrins. Chapter 1 is a review on the applications of porphyrin derivatives and also on the cycloaddition reactions involving the peripheral double bonds of porphyrins. Chapter 2 is related with the 1,3-dipolar cycloaddition reactions of meso-tetraarylporphyrins with azomethine ylides. Firstly, the reactivities of symmetrical meso-tetraarylporphyrins in the reactions with azomethine ylides were investigated; secondly, the 1,3-dipolar cycloaddition reactions of A3B type meso-tetraarylporphyrins with azomethine ylides were also carried out; thirdly, the intramolecular 1,3-dipolar cycloaddition reactions of meso-(o-formylphenyl)porphyrins were also studied. Chapter 3 is related with Diels-Alder reactions of meso-tetraarylporphyrins with pyrazine ortho-quinodimethane. The novel π-extended porphyrins were obtained from the intramolecular ring closure reactions between the meso-aryl group and the β-fused quinoxaline ring. Chapter 4 is related with 1,3-dipolar cycloaddition reactions of porphyrinic pyridinium N-ylides. The reactions of porphyrinic pyridinium N-ylides with quinones and dimethyl acetylenedicarboxylate afford meso-substituted indolizine porphyrins. The quinones were used in excess, acting as dipolarophiles and as oxidants. The novel polycyclic aromatic compounds were obtained from the reactions of porphyrinic pyridinium N-ylides with the electron-deficient alkenes in the absence of any oxidant. Chapter 5 is related with the synthesis of polycyclic aromatic porphyrin analogues via electrocyclic reactions.These novel analogues were synthesized from the reactions of ketone-bridged porphyrins with phosphorus ylides. For the structural characterizations of the new compounds modern analytical techniques were used, with a special emphasis on NMR spectroscopic studies. These NMR methods include 1D: 1H, 13C, DEPT; 2D: COSY, NOESY, HSQC, HMBC.
MacNevin, Christopher J. „Reactivity of substituted 4-Pyridones in normal and inverse demand Diels-Alder cycloaddition /“. Electronic version (PDF), 2003. http://dl.uncw.edu/etd/2003/macnevinc/christophermacnevin.pdf.
Der volle Inhalt der QuelleNagare, A. S. „Physical - organic aspects of diels - alder reactions in eutectic and other environmental benign media“. Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2016. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/5884.
Der volle Inhalt der QuelleCompain-Batissou, Cudel Muriel. „SYNTHESE DE NOUVELLES QUINONES HETEROCYCLIQUES PAR APPLICATION DES REACTIONS DE CYCLOADDITIONS DE DIELS-ALDER ET 1,3-DIPOLAIRE. EVALUATION IN VITRO DE LEUR ACTIVITE SUR TOXOPLASMA GONDII“. Phd thesis, Université Claude Bernard - Lyon I, 2007. http://tel.archives-ouvertes.fr/tel-00281991.
Der volle Inhalt der QuelleBanert, Klaus, Sandra Bochmann, Andreas Ihle, Oliver Plefka, Florian Taubert, Tina Walther, Marcus Korb, Tobias Rüffer und Heinrich Lang. „Synthesis with Perfect Atom Economy: Generation of Furan Derivatives by 1,3-Dipolar Cycloaddition of Acetylenedicarboxylates at Cyclooctynes“. Universitätsbibliothek Chemnitz, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-152891.
Der volle Inhalt der QuelleAlves, Jessica. „Advanced photochemical reaction systems for molecular design“. Thesis, Queensland University of Technology, 2022. https://eprints.qut.edu.au/227734/1/Jessica_Alves_Thesis.pdf.
Der volle Inhalt der QuelleBennes, Raphael Michel. „Recognition-induced control and acceleration of Diels-Alder cycloadditions“. Thesis, University of Birmingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.368517.
Der volle Inhalt der QuelleWijnen, Jan Willem. „Cycloadditions in aqueous media“. [S.l. : [Groningen] : s.n.] ; [University Library Groningen] [Host], 1997. http://irs.ub.rug.nl/ppn/159343356.
Der volle Inhalt der QuelleBücher zum Thema "Diels-Alder cycloaddition reactions"
Hamer, Jan. 1,4-Cycloaddition Reaction : the Diels-Alder Reaction in Heterocyclic Syntheses: The Diels-Alder Reaction in Heterocyclic Syntheses. Elsevier Science & Technology Books, 2013.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Diels-Alder cycloaddition reactions"
Kitamura, Chitoshi. „Synthesis of Substituted Oligoacenes via Diels-Alder Reactions and Substituent Effects on Molecular Structure, Packing Arrangement, and Solid-State Optical Properties“. In Methods and Applications of Cycloaddition Reactions in Organic Syntheses, 407–28. Hoboken, New Jersey: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118778173.ch14.
Der volle Inhalt der QuelleWu, Haoxing, und Neal K. Devaraj. „Inverse Electron-Demand Diels–Alder Bioorthogonal Reactions“. In Cycloadditions in Bioorthogonal Chemistry, 109–30. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-29686-9_6.
Der volle Inhalt der QuelleAbe, M., und T. Yamamoto. „Diels–Alder Cycloaddition Reactions“. In Monocyclic Arenes, Quasiarenes, and Annulenes, 1. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-045-00599.
Der volle Inhalt der QuelleGlass, R. S. „Diels–Alder Cycloaddition Reactions“. In Three Carbon-Heteroatom Bonds: Amides and Derivatives; Peptides; Lactams, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-022-00170.
Der volle Inhalt der Quelle„Intermolecular Diels-Alder Reactions“. In Cycloaddition Reactions in Organic Synthesis, 91–139. Elsevier, 1990. http://dx.doi.org/10.1016/b978-0-08-034712-7.50007-2.
Der volle Inhalt der Quelle„Intramolecular Diels-Alder Reactions“. In Cycloaddition Reactions in Organic Synthesis, 140–208. Elsevier, 1990. http://dx.doi.org/10.1016/b978-0-08-034712-7.50008-4.
Der volle Inhalt der QuelleClayden, Jonathan, Nick Greeves und Stuart Warren. „Pericyclic reactions 1: cycloadditions“. In Organic Chemistry. Oxford University Press, 2012. http://dx.doi.org/10.1093/hesc/9780199270293.003.0034.
Der volle Inhalt der QuelleIan, Fleming. „Cycloaddition reactions“. In Pericyclic Reactions. Oxford University Press, 2015. http://dx.doi.org/10.1093/hesc/9780199680900.003.0002.
Der volle Inhalt der Quelle„2. Diels–Alder cycloaddition reactions“. In High Pressure Organic Synthesis, 23–76. Berlin, Boston: De Gruyter, 2019. http://dx.doi.org/10.1515/9783110556841-002.
Der volle Inhalt der QuelleProcter, Garry. „Additions to C-C double bonds“. In Asymmetric Synthesis, 101–47. Oxford University PressOxford, 1996. http://dx.doi.org/10.1093/oso/9780198557265.003.0006.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Diels-Alder cycloaddition reactions"
Kneeteman, María, Mauro Cainelli, Carla Ormachea und Pedro Mancini. „THEORETICAL STUDY OF POTENTIALLY COMPLEX REACTIONS TO THE CYCLOADDITION PROCESS OF QUINOLINES IN HETERO DIELS-ALDER SYSTEMS.“ In The 19th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-e011.
Der volle Inhalt der QuelleDoležal, Rafael, Natálie Karásková, Nadezhda V. Maltsevskaya und Karel Kolář. „SUPPORTING CONCEPTUAL LEARNING IN ORGANIC CHEMISTRY THROUGH SEMI-EMPIRICAL MOLECULAR MODELING: HEURISTICS OF DIELS-ALDER [4+2] CYCLOADITIONS FOR PREPARATION OF POTENTIAL TLR4 MODULATORS“. In Proceedings of the 2nd International Baltic Symposium on Science and Technology Education (BalticSTE2017). Scientia Socialis Ltd., 2017. http://dx.doi.org/10.33225/balticste/2017.39.
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