Добірка наукової літератури з теми "Allenic ketones"
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Статті в журналах з теми "Allenic ketones"
Bernard, Didier, та Alain Doutheau. "New preparation of α-allenic ketones". Tetrahedron Letters 26, № 40 (січень 1985): 4923–24. http://dx.doi.org/10.1016/s0040-4039(00)94986-4.
Повний текст джерелаFan, Xuesen, Yan He та Xinying Zhang. "Recent Advances in the Reactions of 1,2-Allenic Ketones and α-Allenic Alcohols". Chemical Record 16, № 3 (27 травня 2016): 1635–46. http://dx.doi.org/10.1002/tcr.201500301.
Повний текст джерелаTang, Xiaodong, Huanzhen Ni, and Yixin Lu. "Phosphine-catalyzed enantioselective [4 + 1] annulation of oxindoles with allenic ketones for the construction of spirocyclopentene oxindoles." Organic Chemistry Frontiers 8, no. 16 (2021): 4485–89. http://dx.doi.org/10.1039/d1qo00669j.
Повний текст джерелаLi, Shengxiao, Xin-Xing Wu, and Shufeng Chen. "Base-promoted direct synthesis of functionalized N-arylindoles via the cascade reactions of allenic ketones with indoles." Organic & Biomolecular Chemistry 17, no. 4 (2019): 789–93. http://dx.doi.org/10.1039/c8ob02921k.
Повний текст джерелаWang, Qiang, Tao Zhang, Yunchang Fan, and Xuesen Fan. "Synthesis of functionalized cyclopentenes through allenic ketone-based multicomponent reactions." Organic & Biomolecular Chemistry 16, no. 45 (2018): 8854–58. http://dx.doi.org/10.1039/c8ob02259c.
Повний текст джерелаCrandall, Jack K., and Maher Mualla. "Reductive cyclizations of allenic ketones by dissolving metals." Tetrahedron Letters 27, no. 20 (1986): 2243–46. http://dx.doi.org/10.1016/s0040-4039(00)84497-4.
Повний текст джерелаKanai, M., M. Shibasaki, D. Zhao, and K. Oisaki. "Reductive Aldol Reaction of Allenic Esters to Ketones." Synfacts 2007, no. 2 (February 2007): 0171. http://dx.doi.org/10.1055/s-2006-955837.
Повний текст джерелаTrifonov, Latchezar S., Alexander S. Orahovats, Anthony Linden, and Heinz Heimgartner. "Carbonyliron Complexation and Carbonyl Insertion of Allenic Ketones." Helvetica Chimica Acta 75, no. 6 (October 2, 1992): 1872–79. http://dx.doi.org/10.1002/hlca.19920750613.
Повний текст джерелаWang, Qiang, Xiaonan Shi, Xinying Zhang, and Xuesen Fan. "A convenient synthesis of 1-aryl-1H-1,2,3-triazoles from aliphatic substrates." Org. Biomol. Chem. 15, no. 40 (2017): 8529–34. http://dx.doi.org/10.1039/c7ob02035j.
Повний текст джерелаElsner, Petteri, Luca Bernardi, Giorgio Dela Salla, Jacob Overgaard, and Karl Anker Jørgensen. "Organocatalytic Asymmetric Conjugate Addition to Allenic Esters and Ketones." Journal of the American Chemical Society 130, no. 14 (April 2008): 4897–905. http://dx.doi.org/10.1021/ja710689c.
Повний текст джерелаДисертації з теми "Allenic ketones"
Liu, Renmao. "Asymmetric Dihydroxylation and Aziridination of Allenes and Related Chemistry." BYU ScholarsArchive, 2007. https://scholarsarchive.byu.edu/etd/899.
Повний текст джерелаTellier, Frédérique. "Synthese et reactivite de dienes, enynes et styrenes fluores." Paris 6, 1986. http://www.theses.fr/1986PA066521.
Повний текст джерелаLloyd, Natoiya Dee Rayette. "Synthesis of allenic ketones and the role of yeast in their conversion to damascenone." Thesis, 2013. http://hdl.handle.net/2440/86744.
Повний текст джерелаThesis (Ph.D.) -- University of Adelaide, School of Agriculture, Food and Wine, 2013
Wang, Shu-Huei, and 王淑惠. "Synthesis of Pyrazoles and Isoxazoles from Allenyl Ketones and A New Additional Reaction for Synthesis of b-Halo Ketones." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/85930026189372885183.
Повний текст джерела淡江大學
化學學系博士班
93
Part I: Pyrazole and Isoxazole are well-known as useful synthetic intermediates and important structural units which are widely observed in natural products and biological active molecules. Several methods for synthesis of isoxazoles have been developed and reported and the cyclocondensation reaction of b-diketone with hydroxylamine is one of the most common used method. The limitation of this method is the unsymmetrical b-dicarbonyl compounds can not be prepared regioselectively. The condensation reactions of oxime dianions with esters provide a regioselective accesses to generate b-keto oximes, which then undergo cyclodehydrations to afford isoxazoles. We wish to report a new synthetic method which improves and permits a variety of substituted pyrazoles and isoxazoles are easily prepared. Pyrazoles were synthesized from a reaction mixture of hydrazine dihydrochloride, sodium methylate and allenyl ketone in anhydrous N, N-dimethylformamide at room temperature. Isoxazoles were synthesized from a reaction mixture of hydroxylamine hydrochloride, cesium carbonate and allenyl ketone in anhydrous dimethyl sulfoxide at room temperature. Part II: b-Halo carbonyl compounds are potentially biologically active molecules and important synthetic intermediates in organic synthesis. Recently, our laboratory reported a simple and an effective method for synthesis of a,b-unsaturated ketone which is an useful synthetic precursor for preparation of a,b-unsaturated ketone. A reaction mixture of a,b-unsaturated ketone, boron trichloride and ethylene glycol in dichloromethane was stirred at 0oC and b-chloro ketone was produced in high yield. The b-bromo ketone was obtained as the major product when a reaction mixture of a,b-unsaturated ketone , boron tribromide and ethylene glycol in dichloromethane was stirred at 0oC after 0.5h.
Marx, Vanessa. "Development of the Interrupted Nazarov Cyclization of Allenyl Vinyl Ketones, with Application to the Total Synthesis of the Cyclooctane Natural Product Roseadione." 2011. http://hdl.handle.net/10222/13885.
Повний текст джерелаMoulins, Jonathan. "Synthesis of Heterocycles via Chemoselective Geminal Acylation of 2-Methoxyoxazolidines, E/Z Isomerization in the Metathesis of Allyl Alcohol Derivatives with a First-Generation Ruthenium Catalyst, and Interception of Nazarov Reaction Intermediates of Allenyl Vinyl Ketones with Arenes." 2013. http://hdl.handle.net/10222/37454.
Повний текст джерелаКниги з теми "Allenic ketones"
Klepper, Joerg, and Baerbel Leiendecker. Glut1 Deficiency. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0005.
Повний текст джерелаЧастини книг з теми "Allenic ketones"
Figadre, B., and X. Franck. "Synthesis from Allenes." In Ketones, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-026-00321.
Повний текст джерелаTius, M. A. "With Ketones." In Cumulenes and Allenes, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-044-00308.
Повний текст джерелаSalan, J. "Isomerization of Allene Oxides." In Ketones, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-026-00463.
Повний текст джерелаSalan, J. "Rearrangement of Allene Oxides." In Ketones, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-026-00530.
Повний текст джерелаGandon, V., and M. Malacria. "Dehydration of Ketones." In Cumulenes and Allenes, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-044-00209.
Повний текст джерелаTius, M. A. "With Allenyl Ethers and Ketones." In Cumulenes and Allenes, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-044-00292.
Повний текст джерелаMarsden, S. P. "Transition-Metal-Catalyzed Addition of Aryl Halides and Carbon Monoxide to Allenes." In Ketones, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-026-01037.
Повний текст джерелаOgasawara, M. "Wittig Reaction of Aldehydes or Ketones with Allenylidenephosphoranes." In Cumulenes and Allenes, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-044-00071.
Повний текст джерелаOgasawara, M. "Horner–Emmons-Type Reactions of Aldehydes or Ketones." In Cumulenes and Allenes, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-044-00073.
Повний текст джерелаBrandsma, Lambert. "Reactions with Aldehydes and Ketones." In Synthesis of Acetylenes, Allenes and Cumulenes, 119–34. Elsevier, 2004. http://dx.doi.org/10.1016/b978-012125751-4/50006-0.
Повний текст джерелаТези доповідей конференцій з теми "Allenic ketones"
Poynter, M. E., J. L. Ather, L. F. Reed, M. L. T. Barup, and M. M. Mank. "Ketone Body Augmentation Decreases Methacholine Hyperresponsiveness in a Mouse Model of House Dust Mite-Induced Allergic Asthma." In American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a1297.
Повний текст джерела