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Статті в журналах з теми "Cumulenes; organic compounds synthesis"
Mai, Juri, and Sascha Ott. "The Fascinating World of Phosphanylphosphonates: From Acetylenic Phosphaalkenes to Reductive Aldehyde Couplings." Synlett 30, no. 16 (August 13, 2019): 1867–85. http://dx.doi.org/10.1055/s-0039-1690129.
Повний текст джерелаHopf, Henning, and Georgios Markopoulos. "The chemistry of bisallenes." Beilstein Journal of Organic Chemistry 8 (November 15, 2012): 1936–98. http://dx.doi.org/10.3762/bjoc.8.225.
Повний текст джерелаSantos, Jose, Pavel Jelínek, David Ecija, and Nazario Martin. "(Invited) On-Surface Synthesis of Acene Polymers." ECS Meeting Abstracts MA2022-01, no. 11 (July 7, 2022): 811. http://dx.doi.org/10.1149/ma2022-0111811mtgabs.
Повний текст джерелаGawel, Przemyslaw, Elias A. Halabi, David Schweinfurth, Nils Trapp, Laurent Ruhlmann, Corinne Boudon, and François Diederich. "Synthesis of Dicyano-Substituted Benzo[c]fluorenes from Tetraaryl[3]cumulenes." European Journal of Organic Chemistry 2016, no. 17 (May 30, 2016): 2919–24. http://dx.doi.org/10.1002/ejoc.201600470.
Повний текст джерелаYranzo, Gloria I., José Elguero, Robert Flammang, and Curt Wentrup. "Formation of Cumulenes, Triple-Bonded, and Related Compounds by Flash Vacuum Thermolysis of Five-Membered Heterocycles." European Journal of Organic Chemistry 2001, no. 12 (June 2001): 2209–20. http://dx.doi.org/10.1002/1099-0690(200106)2001:12<2209::aid-ejoc2209>3.0.co;2-x.
Повний текст джерелаMURAHASHI, Shun-Ichi, and Takeshi NAOTA. "Organic synthesis using ruthenium compounds." Journal of Synthetic Organic Chemistry, Japan 46, no. 10 (1988): 930–42. http://dx.doi.org/10.5059/yukigoseikyokaishi.46.930.
Повний текст джерелаKUSAMA, Hiroyuki, and Koichi NARASAKA. "Rhenium Compounds in Organic Synthesis." Journal of Synthetic Organic Chemistry, Japan 54, no. 8 (1996): 644–53. http://dx.doi.org/10.5059/yukigoseikyokaishi.54.644.
Повний текст джерелаSHINOKUBO, Hiroshi, and Koichiro OSHIMA. "Organic Synthesis Using Organomanganese Compounds." Journal of Synthetic Organic Chemistry, Japan 57, no. 1 (1999): 13–23. http://dx.doi.org/10.5059/yukigoseikyokaishi.57.13.
Повний текст джерелаNegishi, Ei-ichi, and Tamotsu Takahashi. "Organozirconium Compounds in Organic Synthesis." Synthesis 1988, no. 01 (1988): 1–19. http://dx.doi.org/10.1055/s-1988-27453.
Повний текст джерелаSadekov, Igor D., B. B. Rivkin, and Vladimir I. Minkin. "Organotellurium Compounds in Organic Synthesis." Russian Chemical Reviews 56, no. 4 (April 30, 1987): 343–54. http://dx.doi.org/10.1070/rc1987v056n04abeh003275.
Повний текст джерелаДисертації з теми "Cumulenes; organic compounds synthesis"
Fitzgerald, Mark. "The mass spectrometric and theoretical study of some cumulene oxides of potential interstellar significance : submitted for the degree of Doctor of Philosophy (Ph.D.) /." Title page, table of contents and abstract only, 2004. http://web4.library.adelaide.edu.au/theses/09PH/09phf5531.pdf.
Повний текст джерелаNewington, Ian M. "Azo-anions in organic synthesis." Thesis, University of Oxford, 1985. http://ora.ox.ac.uk/objects/uuid:690ab891-be13-4582-a029-47974d20adac.
Повний текст джерелаReynolds, Stephen J. "Carbamoylcobalt (III) compounds in organic synthesis." Thesis, University of Nottingham, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.280294.
Повний текст джерелаKim, Byeongmoon 1957. "Asymmetric organic synthesis using organoboron compounds." Thesis, Massachusetts Institute of Technology, 1987. http://hdl.handle.net/1721.1/14679.
Повний текст джерелаHaughey, Simon Anthony. "Chemoenzymatic synthesis of organosulfur compounds." Thesis, Queen's University Belfast, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318731.
Повний текст джерелаKou, Xiaodi. "Synthesis, characterization and reactivity of organic bismuth compounds." Fort Worth, Tex. : Texas Christian University, 2007. http://etd.tcu.edu/etdfiles/available/etd-07312007-125631/unrestricted/kou.pdf.
Повний текст джерелаBuckley, Anne Margaret. "Inorganic-organic layer compounds : synthesis and properties." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.253398.
Повний текст джерелаHamilton, A. L. "Applications of lithium compounds in organic synthesis." Thesis, Swansea University, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.637209.
Повний текст джерелаWang, Haofan. "Synthesis and reactions of organoiron compounds." Diss., The University of Arizona, 2003. http://hdl.handle.net/10150/289994.
Повний текст джерелаIkegami, Toru. "Hypervalent Organobismuth Compounds : Synthesis, Reaction, and Applications to Organic Synthesis." 京都大学 (Kyoto University), 1997. http://hdl.handle.net/2433/86484.
Повний текст джерелаКниги з теми "Cumulenes; organic compounds synthesis"
Brandsma, L. Preparative acetylenic chemistry. 2nd ed. Amsterdam: Elsevier, 1988.
Знайти повний текст джерелаBrandsma, L. Preparative acetylenic chemistry. 2nd ed. Amsterdam: Elsevier, 1988.
Знайти повний текст джерелаWillis, Christine L. Organic synthesis. Oxford: Oxford University Press, 1995.
Знайти повний текст джерелаOrganic synthesis. 2nd ed. Boston: McGraw-Hill, 2002.
Знайти повний текст джерелаOrganic synthesis. New York: McGraw-Hill, 1994.
Знайти повний текст джерелаM, Trost Barry, and International Union of Pure and Applied Chemistry., eds. Stereocontrolled organic synthesis. Oxford: Blackwell Scientific Publications, 1994.
Знайти повний текст джерелаSmith, Michael B. Organic synthesis. New York: McGraw-Hill, 1994.
Знайти повний текст джерелаJean-Paul, Quintard, and Rahm Alain, eds. Tin in organic synthesis. London: Butterworths, 1987.
Знайти повний текст джерела1937-, Murahashi Shunʾichi, ed. Ruthenium in organic synthesis. Weinheim: Wiley-VCH, 2004.
Знайти повний текст джерелаRenu, Aggarwal, ed. Organic synthesis: Special techniques. Boca Raton, FL: CRC Press, 2001.
Знайти повний текст джерелаЧастини книг з теми "Cumulenes; organic compounds synthesis"
Ahluwalia, V. K. "Stereoselective Synthesis." In Stereochemistry of Organic Compounds, 505–61. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-84961-0_18.
Повний текст джерелаVolke, Jiří, and František Liška. "Reactions of Organic Compounds at Electrodes." In Electrochemistry in Organic Synthesis, 45–139. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-78699-0_3.
Повний текст джерелаFagnoni, Maurizio. "CHAPTER 6. Colored Compounds for Eco-sustainable Visible-light Promoted Syntheses." In Sustainable Organic Synthesis, 150–80. Cambridge: Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781839164842-00150.
Повний текст джерелаNorman, Richard, and James M. Coxon. "The syntheses of some naturally occurring compounds." In Principles of Organic Synthesis, 728–90. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2166-8_22.
Повний текст джерелаNorman, Richard, and James M. Coxon. "The synthesis of five-and six-membered heterocyclic compounds." In Principles of Organic Synthesis, 676–727. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2166-8_21.
Повний текст джерелаKostikov, Rafael R., Alexandr P. Molchanov, and Henning Hopf. "Gem-Dihalocyclopropanes in organic synthesis." In Small Ring Compounds in Organic Synthesis IV, 41–80. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/3-540-52422-3_2.
Повний текст джерелаCarl, Elena, and Dietmar Stalke. "Structure-Reactivity Relationship in Organolithium Compounds." In Lithium Compounds in Organic Synthesis, 1–32. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.ch1.
Повний текст джерелаHarrison-Marchand, Anne, and Jacques Maddaluno. "Advances in the Chemistry of Chiral Lithium Amides." In Lithium Compounds in Organic Synthesis, 297–328. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.ch10.
Повний текст джерелаMinko, Yury, and Ilan Marek. "Advances in Carbolithiation." In Lithium Compounds in Organic Synthesis, 329–50. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.ch11.
Повний текст джерелаAzzena, Ugo, and Luisa Pisano. "Reductive Lithiation and Multilithiated Compounds in Synthesis." In Lithium Compounds in Organic Synthesis, 351–74. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.ch12.
Повний текст джерелаТези доповідей конференцій з теми "Cumulenes; organic compounds synthesis"
Monçalves, Matias, Mariana M. Bassaco, Marcos A. Villetti, and Claudio C. Silveira. "Novel Divinyl Sulfides: Potential Luminescent Compounds." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0308-1.
Повний текст джерелаMartins, Lucimara J., Wanessa F. Altei, Cristiane S. Schwalm, Adriano D. Andricopulo, and Fernando Coelho. "Synthesis of new biologically actived azaspiro compounds." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013917144424.
Повний текст джерелаAli, Bakhat, Hélio A. Stefani, and Fernando P. Ferreira. "Addition of Amino Acids to oxopyrrolidin compounds." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20131014161751.
Повний текст джерелаSilva, Anderson B. da, and Juliana A. Vale. "Rapid synthesis of di-1,2,4-oxadiazoles pyridyl compounds." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0031-1.
Повний текст джерелаSilva, Anderson B. da, and Juliana A. Vale. "Rapid synthesis of di-1,2,4-oxadiazoles pyridyl compounds." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0317-1.
Повний текст джерелаCarneiro, Paula F., Maria do Carmo F. R. Pinto, Tatiane S. Coelho, Antonio V. Pinto, Kelly C. G. Moura, Pedro A. da Silva, and Eufrânio N. da Silva Júnior. "Quinonoid and phenazine compounds: synthesis of new antimycobacterial prototypes." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0224-1.
Повний текст джерелаBarbosa, Flavio A. R., Rômulo F. S. Canto, and Antonio L. Braga. "Synthesis of novel 6-seleno-dihydropyrimidinones: Potentially bioactive compounds." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013819222620.
Повний текст джерелаRafique, Jamal, Sumbal Saba, Rômulo F. S. Canto, Waseem Hassan, João B. T. Rocha, and Antonio L. Braga. "Synthesis of Diselenide Based Picolylamide Derivatives: Biologically Potential Compounds." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013822125235.
Повний текст джерелаValdomir, Guillermo, Juan Ignacio Padrón, Jenny Saldaña, José Manuel Padrón, Gloria Serra, Eduardo Manta, Victor S. Martín, and Danilo Davyt. "Synthesis of hybrids compounds by Click Chemistry and their bioactivities." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0081-1.
Повний текст джерелаBrondani, Patrícia B., Gonzalo de Gonzalo, Marco W. Fraaije, and Leandro H. Andrade. "Selective oxidations of organoboron compounds catalyzed by Baeyer-Villiger monooxygenases." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0097-2.
Повний текст джерелаЗвіти організацій з теми "Cumulenes; organic compounds synthesis"
Wiemers, K. D., H. Babad, R. T. Hallen, L. P. Jackson, and M. E. Lerchen. An Assessment of the Stability and the Potential for In-Situ Synthesis of Regulated Organic Compounds in High Level Radioactive Waste Stored at Hanford, Richland, Washington. Office of Scientific and Technical Information (OSTI), January 1999. http://dx.doi.org/10.2172/2535.
Повний текст джерела