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Artykuły w czasopismach na temat "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 i Howard Dalton. "Dioxygenase-catalyzed cis-dihydroxylation of pyridine-ring systems". Canadian Journal of Chemistry 80, nr 6 (1.06.2002): 589–600. http://dx.doi.org/10.1139/v02-062.
Pełny tekst źródłaWilliams, Andrew C. "The synthesis of carbocyclic aromatic systems". Contemporary Organic Synthesis 3, nr 6 (1996): 535. http://dx.doi.org/10.1039/co9960300535.
Pełny tekst źródłaAndo, Wataru. "Polyorganosilicon Compounds in Strained Carbocyclic Systems". Bulletin of the Chemical Society of Japan 69, nr 1 (styczeń 1996): 1–16. http://dx.doi.org/10.1246/bcsj.69.1.
Pełny tekst źródłaGleiter, Rolf, i Daniel B. Werz. "Reactions of Metal-Complexed Carbocyclic 4π Systems". Organometallics 24, nr 18 (sierpień 2005): 4316–29. http://dx.doi.org/10.1021/om0504351.
Pełny tekst źródłaWILLIAMS, A. C. "ChemInform Abstract: The Synthesis of Carbocyclic Aromatic Systems". ChemInform 28, nr 19 (4.08.2010): no. http://dx.doi.org/10.1002/chin.199719292.
Pełny tekst źródłaANDO, W. "ChemInform Abstract: Polyorganosilicon Compounds in Strained Carbocyclic Systems". ChemInform 27, nr 17 (5.08.2010): no. http://dx.doi.org/10.1002/chin.199617312.
Pełny tekst źródłaAl 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, nr 2 (1.05.2024): 318–37. http://dx.doi.org/10.3390/reactions5020016.
Pełny tekst źródłaErian, Ayman W., Yvette A. Issac i Sherif M. Sherif. "A Novel Synthesis of Sulfone Systems as Antimicrobial Agents". Zeitschrift für Naturforschung B 55, nr 1 (1.01.2000): 127–32. http://dx.doi.org/10.1515/znb-2000-0119.
Pełny tekst źródłaDoraghi, Fatemeh, Mohammad Mahdi Aghanour Ashtiani, Fatemeh Moradkhani, Bagher Larijani i Mohammad Mahdavi. "Developments and applications of α-bromonitrostyrenes in organic syntheses". RSC Advances 14, nr 21 (2024): 14835–46. http://dx.doi.org/10.1039/d4ra02474e.
Pełny tekst źródłaWang, Zheng, Yanping Ma, Jingjing Guo, Qingbin Liu, Gregory A. Solan, Tongling Liang i 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, nr 8 (2019): 2582–91. http://dx.doi.org/10.1039/c8dt04892d.
Pełny tekst źródłaRozprawy doktorskie na temat "Carbocyclic systems"
Giustra, Zachary Xavier. "Studies of BN-Isosteres of Carbocyclic Systems". Thesis, Boston College, 2018. http://hdl.handle.net/2345/bc-ir:108092.
Pełny tekst źródłaThe 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.
Pełny tekst źródłaJandl, Christian Verfasser], Roland A. [Akademischer Betreuer] [Fischer, Ullrich [Gutachter] Englert, Polly L. [Gutachter] Arnold i 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.
Pełny tekst źródłaJandl, Christian [Verfasser], Roland A. [Akademischer Betreuer] Fischer, Ullrich [Gutachter] Englert, Polly L. [Gutachter] Arnold i 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.
Pełny tekst źródła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.
Pełny tekst źródła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, i 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.
Pełny tekst źródłaCzęści książek na temat "Carbocyclic systems"
Roy, M. N., V. N. G. Lindsay i A. B. Charette. "Synthesis of Carbocyclic Bicyclo Ring Systems". W 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.
Pełny tekst źródła"2. Benzocyclobutene and Related Systems". W Carbocyclic Three- and Four-Membered Ring Compounds, redaktor Armin de Meijere. Stuttgart: Georg Thieme Verlag, 1997. http://dx.doi.org/10.1055/b-0035-112579.
Pełny tekst źródłaPatrick, Graham L. "Cyclic systems in drug synthesis". W An Introduction to Drug Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/hesc/9780198708438.003.0005.
Pełny tekst źródła"Thiophene Systems Containing Three or More Carbocyclic Fused Rings". W 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.
Pełny tekst źródłaGraham, A., i M. Robinson. "Tricyclic Systems: Central Carbocyclic Ring with Fused Five-membered Rings". W Comprehensive Heterocyclic Chemistry III, 1135–99. Elsevier, 2008. http://dx.doi.org/10.1016/b978-008044992-0.00921-4.
Pełny tekst źródłaBuckley, B. R. "Tricyclic Systems: Central Carbocyclic Ring with Fused Six-membered Rings". W Comprehensive Heterocyclic Chemistry III, 1229–68. Elsevier, 2008. http://dx.doi.org/10.1016/b978-008044992-0.00923-8.
Pełny tekst źródłaConboy, Darren, i Fawaz Aldabbagh. "Tricyclic Systems: Central Carbocyclic Ring With Fused Five-Membered Rings". W Reference Module in Chemistry, Molecular Sciences and Chemical Engineering. Elsevier, 2020. http://dx.doi.org/10.1016/b978-0-12-818655-8.00017-2.
Pełny tekst źródłaMcKinnon, David M. "Tricyclic Systems: Central Carbocyclic Ring with Fused Five-membered Rings". W Comprehensive Heterocyclic Chemistry II, 841–74. Elsevier, 1996. http://dx.doi.org/10.1016/b978-008096518-5.00165-9.
Pełny tekst źródłaNichol, Kenneth J. "Tricyclic Systems: Central Carbocyclic Ring with Fused Six-membered Rings". W Comprehensive Heterocyclic Chemistry II, 921–45. Elsevier, 1996. http://dx.doi.org/10.1016/b978-008096518-5.00167-2.
Pełny tekst źródłaTaber, Douglass. "Enantioselective Organocatalyzed Construction of Carbocyclic Rings". W Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0072.
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