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Статті в журналах з теми "Carbocyclic systems"
Boyd, Derek R., Narain D. Sharma, Ludmila V. Modyanova, Jonathan G. Carroll, John F. Malone, Christopher CR Allen, John TG Hamilton, David T. Gibson, Rebecca E. Parales, and Howard Dalton. "Dioxygenase-catalyzed cis-dihydroxylation of pyridine-ring systems." Canadian Journal of Chemistry 80, no. 6 (June 1, 2002): 589–600. http://dx.doi.org/10.1139/v02-062.
Повний текст джерелаWilliams, Andrew C. "The synthesis of carbocyclic aromatic systems." Contemporary Organic Synthesis 3, no. 6 (1996): 535. http://dx.doi.org/10.1039/co9960300535.
Повний текст джерелаAndo, Wataru. "Polyorganosilicon Compounds in Strained Carbocyclic Systems." Bulletin of the Chemical Society of Japan 69, no. 1 (January 1996): 1–16. http://dx.doi.org/10.1246/bcsj.69.1.
Повний текст джерелаGleiter, Rolf, та Daniel B. Werz. "Reactions of Metal-Complexed Carbocyclic 4π Systems". Organometallics 24, № 18 (серпень 2005): 4316–29. http://dx.doi.org/10.1021/om0504351.
Повний текст джерелаWILLIAMS, A. C. "ChemInform Abstract: The Synthesis of Carbocyclic Aromatic Systems." ChemInform 28, no. 19 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199719292.
Повний текст джерелаANDO, W. "ChemInform Abstract: Polyorganosilicon Compounds in Strained Carbocyclic Systems." ChemInform 27, no. 17 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199617312.
Повний текст джерелаAl Mamari, Hamad H. "Ir-Catalyzed ortho-C-H Borylation of Aromatic C(sp2)-H Bonds of Carbocyclic Compounds Assisted by N-Bearing Directing Groups." Reactions 5, no. 2 (May 1, 2024): 318–37. http://dx.doi.org/10.3390/reactions5020016.
Повний текст джерелаErian, Ayman W., Yvette A. Issac, and Sherif M. Sherif. "A Novel Synthesis of Sulfone Systems as Antimicrobial Agents." Zeitschrift für Naturforschung B 55, no. 1 (January 1, 2000): 127–32. http://dx.doi.org/10.1515/znb-2000-0119.
Повний текст джерелаDoraghi, Fatemeh, Mohammad Mahdi Aghanour Ashtiani, Fatemeh Moradkhani, Bagher Larijani та Mohammad Mahdavi. "Developments and applications of α-bromonitrostyrenes in organic syntheses". RSC Advances 14, № 21 (2024): 14835–46. http://dx.doi.org/10.1039/d4ra02474e.
Повний текст джерелаWang, Zheng, Yanping Ma, Jingjing Guo, Qingbin Liu, Gregory A. Solan, Tongling Liang, and Wen-Hua Sun. "Bis(imino)pyridines fused with 6- and 7-membered carbocylic rings as N,N,N-scaffolds for cobalt ethylene polymerization catalysts." Dalton Transactions 48, no. 8 (2019): 2582–91. http://dx.doi.org/10.1039/c8dt04892d.
Повний текст джерелаДисертації з теми "Carbocyclic systems"
Giustra, Zachary Xavier. "Studies of BN-Isosteres of Carbocyclic Systems." Thesis, Boston College, 2018. http://hdl.handle.net/2345/bc-ir:108092.
Повний текст джерелаThe first three chapters of this dissertation elaborate on certain facets of the isosteric relationship between different types of boron-nitrogen-containing heterocycles and the corresponding all-carbon compounds. In this vein, Chapter 1 describes selective photoisomerization of aromatic 1,2-dihydro-1,2-azaborines to BN-analogues of bicyclo[2.2.0]hexa-2,5-diene (Dewar benzene). In one instance, the photoisomer product was further derivatized into a series of disubstituted cyclobutanes through manipulations of the boron functionality. Chapter 2 discloses a combined experimental/theoretical mechanistic investigation of preliminary hydrogen release from the amine borane unit in a pair of BN-cycloalkanes. In Chapter 3, the kinetics of complementary dehydrogenation of the alkyl units in a BN-cyclohexene derivative are compared with those of related six-membered carbocycles. Chapter 4 treats with the separate subject of enantioselective silylation of glycerol by a catalytic strategy centered around reversible covalent binding of substrate hydroxyl groups
Thesis (PhD) — Boston College, 2018
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Secci, Francesco. "Strained carbocyclic systems in the synthesis of bioactive products : methodologies and total synthesis." Paris 11, 2006. http://www.theses.fr/2006PA112296.
Повний текст джерелаJandl, Christian Verfasser], Roland A. [Akademischer Betreuer] [Fischer, Ullrich [Gutachter] Englert, Polly L. [Gutachter] Arnold, and Roland A. [Gutachter] Fischer. "Carbocyclic Carbenes and Beyond: Functionalised Cycloheptatriene Systems as Versatile Ligands in Palladium Chemistry / Christian Jandl ; Gutachter: Ullrich Englert, Polly L. Arnold, Roland A. Fischer ; Betreuer: Roland A. Fischer." München : Universitätsbibliothek der TU München, 2018. http://nbn-resolving.de/urn:nbn:de:bvb:91-diss-20180215-1398715-1-5.
Повний текст джерелаJandl, Christian [Verfasser], Roland A. [Akademischer Betreuer] Fischer, Ullrich [Gutachter] Englert, Polly L. [Gutachter] Arnold, and Roland A. [Gutachter] Fischer. "Carbocyclic Carbenes and Beyond: Functionalised Cycloheptatriene Systems as Versatile Ligands in Palladium Chemistry / Christian Jandl ; Gutachter: Ullrich Englert, Polly L. Arnold, Roland A. Fischer ; Betreuer: Roland A. Fischer." München : Universitätsbibliothek der TU München, 2018. http://d-nb.info/1153545837/34.
Повний текст джерела薩加. "The Transition Metal Catalyzed New Organic Transformation of Enynes for Synthesis of Highly Functionalized Carbocyclic & Heterocyclic Systems." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/73839021793932674798.
Повний текст джерела國立清華大學
化學系
102
This dissertation describes the development of new synthetic organic transformation by using gold and zinc salts. Transition metal-catalyzed organic transformations such as Oxidative Cyclization, Di-stereo and Enatioselective [2+2+3] cycloaddition, 1,4-Dioxo Functionalizations, 1,4-Metathesis Reactions of appropriately functionalized organic molecules are described in this dissertation. For sake of convenience and better understanding, the thesis is divided into four chapters. The first chapter deals with the Gold-Catalyzed Oxidative Cyclization of 1,5-Enynes Using External Oxidants (8-Methylquinoline N-Oxide) to deliver indanone frameworks. Such indanone core is one of the most commonly encountering skeletons in nature. The core structure of the resulting products are construct through a formal reactions proceed through prior oxidations of alkyne to form α-carbonyl intermediates, followed by intramolecular carbocyclizations. The second chapter deals with the Gold-catalyzed diastereo- and enantioselective [2+2+3]-cycloaddition reactions of 1,6-enynes with nitrones. The utility of such reactions is manifested by a wide substrate scopes of 1,6-enynes and nitrones. This Gold-catalyzed diastereo- and enantioselective [2+2+3]-cycloaddition reactions of 1,6-enynes with nitrones deliver 1,2-Oxazepane core which has wide aplication in structural and biological importance. The third chapter describes new 1,4-oxo functionalizations of 3-en-1-ynes based on a hydrative oxidation approach. The one-pot dioxo reactions were applicable to various 3-en-1-ynes including unactivated 3-aryl-3-en-1-ynes, giving Z- or E-configured 2-en-1,4-dicarbonyl compounds selectively. In this chapter, mechanistic analysis supported an initial formation of furan intermediates, generated from carbonyl-assisted alkenyl fluorinations of hydration intermediates. This work reports the first success for 1,4-oxo functionations of readily available 3-en-1-ynes to offer highly functionalized alkenes. The fourth chapter presents Catalyst-dependent metathesis reactions between 3-en-1-ynamides and nitrosoarenes are described. Particularly notable are the unprecedented 1,4-metathesis reactions catalyzed by Ag(I) or Zn(II) to give 3-imidoylalkynes and benzaldehyde. With 3-en-1-ynamides bearing a cycloalkenyl group, 1,4-oxoimination products were produced efficiently without molecular fragmentation. We have developed metathesis/alkynation cascades for terminal 3-imidoylalkynes and benzaldehyde species generated in situ, to manifest 1,4-hydroxyimination reactions of 3-en-1-ynes.
Baburao, Huple Deepak, and 迪帕. "Synthesis of Heterocyclic &; Carbocyclic Systems via Silver and Gold Catalyzed [3+2],[4+2]and [2+2+2]-Cycloadditions &; Oxidative Cyclization." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/97878077621973421785.
Повний текст джерелаЧастини книг з теми "Carbocyclic systems"
Roy, M. N., V. N. G. Lindsay, and A. B. Charette. "Synthesis of Carbocyclic Bicyclo Ring Systems." In Stereoselective Synthesis 1 Stereoselective Reactions of Carbon—Carbon Double Bonds, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-201-00409.
Повний текст джерела"2. Benzocyclobutene and Related Systems." In Carbocyclic Three- and Four-Membered Ring Compounds, edited by Armin de Meijere. Stuttgart: Georg Thieme Verlag, 1997. http://dx.doi.org/10.1055/b-0035-112579.
Повний текст джерелаPatrick, Graham L. "Cyclic systems in drug synthesis." In An Introduction to Drug Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/hesc/9780198708438.003.0005.
Повний текст джерела"Thiophene Systems Containing Three or More Carbocyclic Fused Rings." In Chemistry of Heterocyclic Compounds: A Series Of Monographs, 315–55. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186565.ch6.
Повний текст джерелаGraham, A., and M. Robinson. "Tricyclic Systems: Central Carbocyclic Ring with Fused Five-membered Rings." In Comprehensive Heterocyclic Chemistry III, 1135–99. Elsevier, 2008. http://dx.doi.org/10.1016/b978-008044992-0.00921-4.
Повний текст джерелаBuckley, B. R. "Tricyclic Systems: Central Carbocyclic Ring with Fused Six-membered Rings." In Comprehensive Heterocyclic Chemistry III, 1229–68. Elsevier, 2008. http://dx.doi.org/10.1016/b978-008044992-0.00923-8.
Повний текст джерелаConboy, Darren, and Fawaz Aldabbagh. "Tricyclic Systems: Central Carbocyclic Ring With Fused Five-Membered Rings." In Reference Module in Chemistry, Molecular Sciences and Chemical Engineering. Elsevier, 2020. http://dx.doi.org/10.1016/b978-0-12-818655-8.00017-2.
Повний текст джерелаMcKinnon, David M. "Tricyclic Systems: Central Carbocyclic Ring with Fused Five-membered Rings." In Comprehensive Heterocyclic Chemistry II, 841–74. Elsevier, 1996. http://dx.doi.org/10.1016/b978-008096518-5.00165-9.
Повний текст джерелаNichol, Kenneth J. "Tricyclic Systems: Central Carbocyclic Ring with Fused Six-membered Rings." In Comprehensive Heterocyclic Chemistry II, 921–45. Elsevier, 1996. http://dx.doi.org/10.1016/b978-008096518-5.00167-2.
Повний текст джерелаTaber, Douglass. "Enantioselective Organocatalyzed Construction of Carbocyclic Rings." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0072.
Повний текст джерела