Добірка наукової літератури з теми "Dienophiles"
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Статті в журналах з теми "Dienophiles"
Talma, A. G., R. N. Datta, and J. Aerts. "Quantum Mechanical Calculations to Assess the Antireversion Effects of Several Dienophiles." Rubber Chemistry and Technology 74, no. 4 (September 1, 2001): 574–82. http://dx.doi.org/10.5254/1.3544958.
Повний текст джерелаOmar, Yasser M., Giulia Santucci, and Kamyar Afarinkia. "tert-Butyl(2-oxo-2H-pyran-5-yl)carbamate as the First Chameleon Diene Bearing an Electron-Donating Substituent." Molecules 27, no. 17 (September 2, 2022): 5666. http://dx.doi.org/10.3390/molecules27175666.
Повний текст джерелаSu, Zhishan, and Chan Kyung Kim. "Trienamine catalysis for asymmetric Diels–Alder reactions of 2,4-dienones: a theoretical investigation." Organic & Biomolecular Chemistry 13, no. 22 (2015): 6313–24. http://dx.doi.org/10.1039/c5ob00797f.
Повний текст джерелаSeo, Jeong-Min, and Jong-Beom Baek. "A solvent-free Diels–Alder reaction of graphite into functionalized graphene nanosheets." Chem. Commun. 50, no. 93 (2014): 14651–53. http://dx.doi.org/10.1039/c4cc07173e.
Повний текст джерелаWard, Dale E., Thomas E. Nixey, Yuanzhu Gai, Matthew J. Hrapchak, and M. Saeed Abaee. "Intramolecular Diels–Alder reactions of 2H-thiopyran dienes." Canadian Journal of Chemistry 74, no. 7 (July 1, 1996): 1418–36. http://dx.doi.org/10.1139/v96-160.
Повний текст джерелаLiu, Hsing-Jang, Dan-Xiong Wang, Jeung Bea Kim, Eric N. C. Browne, and Yu Wang. "Activated cyclooctenones are effective dienophiles." Canadian Journal of Chemistry 75, no. 6 (June 1, 1997): 899–912. http://dx.doi.org/10.1139/v97-108.
Повний текст джерелаLiu, Zhang, Wang, Zan, and Zhang. "The Role of Iodine Catalyst in the Synthesis of 22-Carbon Tricarboxylic Acid and Its Ester: A Case Study." Catalysts 9, no. 12 (November 20, 2019): 972. http://dx.doi.org/10.3390/catal9120972.
Повний текст джерелаNdibwami, Alexis, Serge Lamothe, Daniel Guay, Raymond Plante, Pierre Soucy, Solo Goldstein, and Pierre Deslongchamps. "Transannular Diels–Alder reactions on 14-membered macrocyclic trienes. Part I: stereoselective syntheses of the macrocyclic trienes precursors." Canadian Journal of Chemistry 71, no. 5 (May 1, 1993): 695–713. http://dx.doi.org/10.1139/v93-094.
Повний текст джерелаBarta, Petra, Ferenc Fülöp, and István Szatmári. "Mannich base-connected syntheses mediated by ortho-quinone methides." Beilstein Journal of Organic Chemistry 14 (March 6, 2018): 560–75. http://dx.doi.org/10.3762/bjoc.14.43.
Повний текст джерелаThiessen, Merlina, and Volker Abetz. "Influence of the Glass Transition Temperature and the Density of Crosslinking Groups on the Reversibility of Diels-Alder Polymer Networks." Polymers 13, no. 8 (April 7, 2021): 1189. http://dx.doi.org/10.3390/polym13081189.
Повний текст джерелаДисертації з теми "Dienophiles"
Siberdt, Fabian. "Action de dienophiles sur les 2-vinylindolizines." Doctoral thesis, Universite Libre de Bruxelles, 1995. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/212576.
Повний текст джерелаLochrie, Ian Stewart Tolmie. "Investigation of diastereomeric induction in the Diels-Alder reactions of acylnitroso dienophiles." Thesis, University of Glasgow, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.320289.
Повний текст джерелаYoussofi, Abdullah. "Etude des dichloroboranes vinyliques en tant que dienophiles. Application a la synthese stereocontrolee d'heterocycles bicycliques azotes et oxygenes." Rennes 1, 1994. http://www.theses.fr/1994REN10186.
Повний текст джерелаLAMEIGNERE, ERIC. "Synthese de dienes et de dienophiles pyranosidiques en vue de leur utilisation dans la synthese de molecules naturelles polycycliques." Paris 11, 1990. http://www.theses.fr/1990PA112032.
Повний текст джерелаHaquin, Catherine. "Diaza-1,3 butadienes et isothiocyanates d'imidoyle : cycloaddition (1+4) avec les isonitriles et cycloaddition (2+4) avec quelques dienophiles electrophiles." Rennes 1, 1987. http://www.theses.fr/1987REN10036.
Повний текст джерелаYu, Jianguo. "Novel chiral phosphonium ionic liquids as solvents and catalysts for cycloadditions : investigation of the Diels-Alder reaction of a series of dienes and dienophiles in novel chiral phosphonium ionic liquids." Thesis, University of Bradford, 2009. http://hdl.handle.net/10454/4307.
Повний текст джерелаNewbury, Daniel John. "Part A: Progress Towards the Total Synthesis of (±)-Communesin F; Part B: Aluminum as a Catalyst for the Diels-Alder Cycloaddition of Highly Hindered Dienophiles." Thèse, Université d'Ottawa / University of Ottawa, 2013. http://hdl.handle.net/10393/23943.
Повний текст джерелаCHAPTAL-GRADOZ, NATHALIE. "Regio et stereoselectivite de reactions de diels-alder entre des dienes portant un substituant allylique chiral en position deux et divers dienophiles. Applications." Paris 11, 1993. http://www.theses.fr/1993PA112310.
Повний текст джерелаByeon, Chang-Ho. "Part I. Reactions of alpha,beta-unsaturated thioesters and selenoesters with enamines :Part II. Alpha,beta-unsaturated thioesters and selenoesters as dienophiles :Synthesis of cyclohexene derivatives /." The Ohio State University, 1994. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487856076418125.
Повний текст джерелаPerkins, Jonathan Clarence. "Synthesis of [2.2.2]-Diazabicyclic Alkaloids: I: Diels-Alder Reactions of a C2-Carboxy Pyrazinone & Ii: Intermolecular Diels-Alder Reaction of a Proline Derived Pyrazinone with Symmetric Dienophiles." W&M ScholarWorks, 2017. https://scholarworks.wm.edu/etd/1516639679.
Повний текст джерелаКниги з теми "Dienophiles"
Hutchinson, Donna Kaye T. *. 3-sulfinylthiochromin-4-one and its Diels-Alder reactions with electron-rich dienophiles. 1988.
Знайти повний текст джерелаЧастини книг з теми "Dienophiles"
Franck, Richard W. "Carbohydrate Dienophiles in [4 + 2] Cycloadditions." In ACS Symposium Series, 24–32. Washington, DC: American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0494.ch002.
Повний текст джерелаBauld, N. L. "Direct and Indirect Diels-Alder Additions to Electron Rich Dienophiles." In Organic Free Radicals, 7–8. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73963-7_4.
Повний текст джерелаCheraitia, Abdallah, and Nawal Brahimi. "Realization of Diene Dienophile Interface Reaction in Oil/Water Emulsion." In Proceedings of the Third International Symposium on Materials and Sustainable Development, 25–33. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-89707-3_4.
Повний текст джерелаOh, Teresa, Kwang Man Lee, Kyung Sik Kim, Sung Bo Oh, Won Hyung Kim, and Chi Kyu Choi. "HOMO-LUMO Interaction between Diene and Dienophile with an Electron-Withdrawing Group." In Key Engineering Materials, 983–89. Stafa: Trans Tech Publications Ltd., 2005. http://dx.doi.org/10.4028/0-87849-958-x.983.
Повний текст джерела"Imino Dienophiles." In Organic Chemistry, 34–70. Elsevier, 1987. http://dx.doi.org/10.1016/b978-0-08-091697-2.50005-6.
Повний текст джерела"Carbonyl Dienophiles." In Organic Chemistry, 94–119. Elsevier, 1987. http://dx.doi.org/10.1016/b978-0-08-091697-2.50007-x.
Повний текст джерела"Miscellaneous Dienophiles." In Organic Chemistry, 146–66. Elsevier, 1987. http://dx.doi.org/10.1016/b978-0-08-091697-2.50009-3.
Повний текст джерела"Nitroso and Thionitroso Dienophiles." In Organic Chemistry, 71–93. Elsevier, 1987. http://dx.doi.org/10.1016/b978-0-08-091697-2.50006-8.
Повний текст джерела"Thiocarbonyl and Selenocarbonyl Dienophiles." In Organic Chemistry, 120–45. Elsevier, 1987. http://dx.doi.org/10.1016/b978-0-08-091697-2.50008-1.
Повний текст джерелаVaultier, M., and G. Alcaraz. "From Dienylboronates and Dienophiles." In Boron Compounds, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-006-00698.
Повний текст джерелаТези доповідей конференцій з теми "Dienophiles"
Mancini, Pedro, Claudia Della Rosa, Elisa Paredes, and María Kneeteman. "2-Nitrofurans as Dienophiles in Diels-Alder Reactions." In The 8th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2004. http://dx.doi.org/10.3390/ecsoc-8-01950.
Повний текст джерелаDib, Salima, Bachir Mostefa-Kara, Didier Villemin, and Nathalie Bar. "Study of Diels–Alder Reactions of Purpurogallin Tetraacetate with Various Dienophiles." In ECSOC-25. Basel Switzerland: MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11707.
Повний текст джерелаTaylor, Richard, Katherine Taylor, and Christopher Goins. "Diels-Alder Reactions of Dienophiles and Cyclopentadiene Using a Sealed Tube Protocol." In The 15th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00698.
Повний текст джерелаKneeteman, Maria. "Nitro-pyridines as Dienophiles in Polar Diels-alder Reactions. A DFT Theoretical Study." In The 16th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01086.
Повний текст джерелаMancini, Pedro, María Kneeteman, and Silvina Cancian. "Nitroquinolines as dienophiles in polar Diels-Alder reactions. Influences of molecular solvents and ionic liquids." In The 14th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00476.
Повний текст джерелаMancini, Pedro Maximo, Claudia Della Rosa, and Maria Kneeteman. "N-tosyl-nitropyrroles as dienophiles in polar cycloaddition reactions developed in protic ionic liquids." In The 15th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00636.
Повний текст джерелаKneeteman, Maria, Pedro Mancini, and Carla Ormachea. "A THEORETICAL ANALISYS OF THE REACTIVITY OF ACYL AZAHETEROCYCLES AS DIENOPHILES IN CYCLOADDITION REACTIONS ." In The 21st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04732.
Повний текст джерелаKneeteman, María, Pedro Mancini, Juan Sanchez, and Claudia Della Rosa. "2-Nitrobenzofuran and 3-Nitrobenzofurans as dienophiles in Polar Diels-Alder Reactions. Theoretical studies using DFT Methods." In The 14th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00473.
Повний текст джерелаMancini, Pedro M. E., Maria N. Kneeteman, and Claudia Della Rosa. "Ionic Liquids and Microwave Irradiation as Synergistic Combination for Polar Diels-Alder Reactions Using Properly Substituted Heterocycles as Dienophiles." In The 16th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01044.
Повний текст джерелаThiemann, Thies, Hasnaa Sadeq, John Graham, Yosef Al Jasem, Bernhard Bugenhagen, and Nathir Al-Rawashdeh. "Photochemistry of 9-Vinyl Substituted Anthracenes of Their Reduced Derivatives and of Diels Alder Type Adducts of 9-Vinylanthracenes With Activated Dienophiles." In The 19th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a037.
Повний текст джерела