Статті в журналах з теми "Cp2TiCl"
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Cozak, Daniel, Abdelhakim Mardhy та André Morneau. "Titanocene derivatives of purine and adenine. Synthesis and characterization of reaction products with (η5-C5H5)2Ti(CO)2, (η5-C5H5)2TiCl, and (η5-C5H5)2TiCl2". Canadian Journal of Chemistry 64, № 4 (1 квітня 1986): 751–59. http://dx.doi.org/10.1139/v86-121.
Повний текст джерелаMaué, Paul G., and Dieter Fenske. "Zur Reaktion von [Cp2TiCl2] und [CpTiCl3] mit E(SiMe3)2 (E = S, Se) Die Kristallstrukturen von [Cp3Ti2S2Cl], [Cp4Ti2S2Cl2], [Cp3Ti2Se2Cl] und [Cp4Ti4Se7O] / Reaction of [Cp2TiCl2] and [CpTiCl3 ] with E(SiMe 3)2 (E = S. Se) The Crystal Structures of [Cp3Ti2S2Cl], [Cp3Ti2S2Cl2], [Cp3Ti2Se2Cl] and [Cp4Ti4Se7O]." Zeitschrift für Naturforschung B 43, no. 10 (October 1, 1988): 1213–18. http://dx.doi.org/10.1515/znb-1988-1001.
Повний текст джерелаThewalt, Ulf, and Reinhard Friedrich. "Cp2TiIV-Komplexe mit Oximatoliganden / Cp2TiIV Complexes with Oximato Ligands." Zeitschrift für Naturforschung B 46, no. 4 (April 1, 1991): 475–82. http://dx.doi.org/10.1515/znb-1991-0409.
Повний текст джерелаBreunig, H. J., O. Moldovan, M. Nema, U. Rosenthal, C. I. Rat, and R. A. Varga. "Formation of [Cp2TiSbMe2]2, [Cp2TiSb(SiMe3)2]2 and [Cp2TiCl]2·2Mes4Sb2." Journal of Organometallic Chemistry 696, no. 2 (January 2011): 523–26. http://dx.doi.org/10.1016/j.jorganchem.2010.09.007.
Повний текст джерелаSrivastava, A. K., O. P. Pandey, and S. K. Sengupta. "Synthesis, Spectral and Antimicrobial Studies of Bis(cyclopentadienyl)titanium(IV) Derivatives with Schiff Bases Derived from 2-Amino-5-phenyl-1,3,4-thiadiazole." Bioinorganic Chemistry and Applications 3, no. 3-4 (2005): 289–97. http://dx.doi.org/10.1155/bca.2005.289.
Повний текст джерелаRosales, Jennifer, Gustavo Cabrera, and José Justicia. "Exploring Short and Efficient Synthetic Routes Using Titanocene(III)-Catalyzed Reactions: Total Synthesis of Natural Meroterpenes with Trisubstituted Unsaturations." Molecules 27, no. 8 (April 8, 2022): 2400. http://dx.doi.org/10.3390/molecules27082400.
Повний текст джерелаSong, Li-Cheng, Cong Han, Qing-Mei Hu, and Zhi-Pan Zhang. "Synthesis of new organotitanium (IV) complexes Cp2Ti(SeR)2 and Cp2TiCl(SeR) via tandem reactions involving `Cp2Ti' intermediate. Crystal structures of Cp2TiCl(SeR) (R=p-ClC6H4, p-BrC6H4)." Inorganica Chimica Acta 357, no. 8 (June 2004): 2199–204. http://dx.doi.org/10.1016/j.ica.2003.06.011.
Повний текст джерелаRosales Martínez, Antonio, Juan F. García-Martín, and Ignacio Rodríguez-García. "Cp2TiCl/H2O as a Sustainable System for the Reduction of Organic Functional Groups: Potential Application of Cp2TiCl/D2O to the Analysis of Bioactive Phenols in Olive Oil." Processes 11, no. 4 (March 23, 2023): 979. http://dx.doi.org/10.3390/pr11040979.
Повний текст джерелаRosales, Antonio, and Ignacio Rodríguez-García. "Cp2TiCl/D2O/Mn, a formidable reagent for the deuteration of organic compounds." Beilstein Journal of Organic Chemistry 12 (July 25, 2016): 1585–89. http://dx.doi.org/10.3762/bjoc.12.154.
Повний текст джерелаCastro Rodríguez, María, Ignacio Rodríguez García, Roman Nicolay Rodríguez Maecker, Laura Pozo Morales, J. Enrique Oltra, and Antonio Rosales Martínez. "Cp2TiCl: An Ideal Reagent for Green Chemistry?" Organic Process Research & Development 21, no. 7 (June 22, 2017): 911–23. http://dx.doi.org/10.1021/acs.oprd.7b00098.
Повний текст джерелаGordon, Jonathan, Sven Hildebrandt, Kendra R. Dewese, Sven Klare, Andreas Gansäuer, T. V. RajanBabu, and William A. Nugent. "Demystifying Cp2Ti(H)Cl and Its Enigmatic Role in the Reactions of Epoxides with Cp2TiCl." Organometallics 37, no. 24 (November 30, 2018): 4801–9. http://dx.doi.org/10.1021/acs.organomet.8b00793.
Повний текст джерелаMorcillo, Sara P., Delia Miguel, Araceli G. Campaña, Luis Álvarez de Cienfuegos, José Justicia, and Juan M. Cuerva. "Recent applications of Cp2TiCl in natural product synthesis." Org. Chem. Front. 1, no. 1 (2014): 15–33. http://dx.doi.org/10.1039/c3qo00024a.
Повний текст джерелаKool, Lawrence B., Marvin D. Rausch, Helmut G. Alt, Max Herberhold, Brigitte Wolf, and Ulf Thewalt. "Structural and spectroscopic comparison of the complexes Cp2M(PMe3)(CO) (M = Ti, Zr, Hf), (C9H7)2Ti(PMe3)(CO) and Cp2TiCl(PMe3); X-ray structures of Cp2Ti(PMe3)(CO) and Cp2TiCl(PMe3)." Journal of Organometallic Chemistry 297, no. 2 (December 1985): 159–69. http://dx.doi.org/10.1016/0022-328x(85)80414-9.
Повний текст джерелаRosales Martínez, Antonio. "Cp2TiCl is a useful reagent to teach multidisciplinary chemistry." Educación Química 32, no. 5 (October 4, 2021): 191. http://dx.doi.org/10.22201/fq.18708404e.2021.5.77418.
Повний текст джерелаHardouin, Christophe, Floris Chevallier, Bernard Rousseau та Eric Doris. "Cp2TiCl-Mediated Selective Reduction of α,β-Epoxy Ketones". Journal of Organic Chemistry 66, № 3 (лютий 2001): 1046–48. http://dx.doi.org/10.1021/jo001358g.
Повний текст джерелаMonleón, Laura M., Manuel Grande, and Josefa Anaya. "Radical cyclisation of epoxynitrile-2-azetidinones mediated by Cp2TiCl." Tetrahedron 63, no. 14 (April 2007): 3017–25. http://dx.doi.org/10.1016/j.tet.2007.01.049.
Повний текст джерелаMoisan, Lionel, Christophe Hardouin, Bernard Rousseau та Eric Doris. "Cp2TiCl-mediated selective reduction of α,β-unsaturated ketones". Tetrahedron Letters 43, № 11 (березень 2002): 2013–15. http://dx.doi.org/10.1016/s0040-4039(02)00170-3.
Повний текст джерелаHansen, Thomas, Sussie L. Krintel, Kim Daasbjerg, and Troels Skrydstrup. "A convenient synthesis of glycals employing in-situ generated Cp2TiCl." Tetrahedron Letters 40, no. 33 (August 1999): 6087–90. http://dx.doi.org/10.1016/s0040-4039(99)01266-6.
Повний текст джерелаMárquez, Irene R., Alba Millán, Araceli G. Campaña, and Juan M. Cuerva. "Cp2TiCl-catalyzed highly stereoselective intramolecular epoxide allylation using allyl carbonates." Org. Chem. Front. 1, no. 4 (2014): 373–81. http://dx.doi.org/10.1039/c4qo00012a.
Повний текст джерелаRosales Martínez, Antonio, Laura Pozo Morales, and Emilio Díaz Ojeda. "Cp2TiCl-catalyzed, concise synthetic approach to marine natural product (±)-cyclozonarone." Synthetic Communications 49, no. 19 (July 9, 2019): 2554–60. http://dx.doi.org/10.1080/00397911.2019.1633671.
Повний текст джерелаMorcillo, Sara P., Delia Miguel, Araceli G. Campana, Luis Alvarez de Cienfuegos, Jose Justicia, and Juan M. Cuerva. "ChemInform Abstract: Recent Applications of Cp2TiCl in Natural Product Synthesis." ChemInform 45, no. 25 (June 5, 2014): no. http://dx.doi.org/10.1002/chin.201425250.
Повний текст джерелаAsandei, Alexandru D., and Gobinda Saha. "Cp2TiCl-catalyzed living radical polymerization of styrene initiated from peroxides." Journal of Polymer Science Part A: Polymer Chemistry 44, no. 3 (2005): 1106–16. http://dx.doi.org/10.1002/pola.21206.
Повний текст джерелаGrande, Manuel, Laura Monleón та Josefa Anaya. "Acyl Radicals from Nitriles Promoted by Cp2TiCl in β-Lactam Chemistry". Synlett 2010, № 08 (15 квітня 2010): 1227–30. http://dx.doi.org/10.1055/s-0029-1219830.
Повний текст джерелаGrande, Manuel, Laura Monleón, and Josefa Anaya. "Approach to Substituted Methylcarbapenems and Benzocarbacephems by Radical Cyclization Using Cp2TiCl." Synlett 2007, no. 08 (May 8, 2007): 1243–46. http://dx.doi.org/10.1055/s-2007-980336.
Повний текст джерелаMoisan, Lionel, Christophe Hardouin, Bernard Rousseau та Eric Doris. "ChemInform Abstract: Cp2TiCl-Mediated Selective Reduction of α,β-Unsaturated Ketones." ChemInform 33, № 26 (21 травня 2010): no. http://dx.doi.org/10.1002/chin.200226051.
Повний текст джерелаHardouin, Christophe, Floris Chevallier, Bernard Rousseau та Eric Doris. "ChemInform Abstract: Cp2TiCl-Mediated Selective Reduction of α,β-Epoxy Ketones." ChemInform 32, № 27 (25 травня 2010): no. http://dx.doi.org/10.1002/chin.200127105.
Повний текст джерелаParadas, Miguel, Araceli G. Campaña, Maria Luisa Marcos, Jose Justicia, Ali Haidour, Rafael Robles, Diego J. Cárdenas, J. Enrique Oltra, and Juan M. Cuerva. "Unprecedented H-atom transfer from water to ketyl radicals mediated by Cp2TiCl." Dalton Transactions 39, no. 37 (2010): 8796. http://dx.doi.org/10.1039/c001689f.
Повний текст джерелаHansen, Thomas, Sussie L. Krintel, Kim Daasbjerg, and Troels Skrydstrup. "ChemInform Abstract: A Convenient Synthesis of Glycals Employing in situ Generated Cp2TiCl." ChemInform 30, no. 44 (June 13, 2010): no. http://dx.doi.org/10.1002/chin.199944233.
Повний текст джерелаSpencer, Roxanne P., and Jeffrey Schwartz. "Variously substituted glycals are readily prepared from glycosyl bromides using (Cp2TiCl)2." Tetrahedron Letters 37, no. 25 (June 1996): 4357–60. http://dx.doi.org/10.1016/0040-4039(96)00865-9.
Повний текст джерелаBermejo, Francisco, and Celso Sandoval. "Cp2TiCl-Promoted Isomerization of Trisubstituted Epoxides toexo-Methylene Allylic Alcohols on Carvone Derivatives." Journal of Organic Chemistry 69, no. 16 (August 2004): 5275–80. http://dx.doi.org/10.1021/jo049358u.
Повний текст джерелаAsandei, Alexandru D., Yanhui Chen, Gobinda Saha, and Isaac W. Moran. "Cp2TiCl-catalyzed radical chemistry: living styrene polymerizations from epoxides, aldehydes, halides, and peroxides." Tetrahedron 64, no. 52 (December 2008): 11831–38. http://dx.doi.org/10.1016/j.tet.2008.08.106.
Повний текст джерелаBegum, Sabnam, and Tushar Kanti Chakraborty. "Cp2TiCl-Mediated Reductive Cyclization: Total Synthesis of Pestalotiolactone A, Myrotheciumone A, and Scabrol A." Journal of Organic Chemistry 86, no. 17 (August 2, 2021): 11812–21. http://dx.doi.org/10.1021/acs.joc.1c01243.
Повний текст джерелаKhan, Hina P. A., and Tushar Kanti Chakraborty. "Application of Cp2TiCl-Promoted Radical-Induced Cyclization: An Expeditious Access to [a]-Annelated Indoles." Journal of Organic Chemistry 85, no. 12 (May 29, 2020): 8000–8012. http://dx.doi.org/10.1021/acs.joc.0c00817.
Повний текст джерелаAsandei, Alexandru D., and Yanhui Chen. "Cp2TiCl-Catalyzed SET Reduction of Aldehydes: A New Initiating Protocol for Living Radical Polymerization." Macromolecules 39, no. 22 (October 2006): 7549–54. http://dx.doi.org/10.1021/ma0604791.
Повний текст джерелаAsandei, Alexandru D., and Gobinda Saha. "Cp2TiCl-Catalyzed Epoxide Radical Ring Opening: A New Initiating Methodology for Graft Copolymer Synthesis." Macromolecules 39, no. 26 (December 2006): 8999–9009. http://dx.doi.org/10.1021/ma0618833.
Повний текст джерелаSPENCER, R. P., and J. SCHWARTZ. "ChemInform Abstract: Variously Substituted Glycals Are Readily Prepared from Glycosyl Bromides Using (Cp2TiCl)2." ChemInform 27, no. 41 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199641205.
Повний текст джерелаvon Gudenberg, Dorothea Wolff, Hak-Chul Kang, Werner Massa, Kurt Dehnicke, C�cilia Maichle-M�ssmer, and Joachim Str�hle. "Silanolato-Komplexe von Titan und Zirconium. Die Kristallstrukturen von Cp2TiCl(OSiPh3) und Cp2ZrCl(OSiPh3)." Zeitschrift f�r anorganische und allgemeine Chemie 620, no. 10 (October 1994): 1719–24. http://dx.doi.org/10.1002/zaac.19946201010.
Повний текст джерелаFenske, D., A. Grissinger, E. M. Hey-Hawkins, and J. Magull. "Zur Reaktion von [Cp2TiCl]2 und TiCl4 mit LiE(SiMe3)2 (E = P, As) und P(SiMe3)3 Die Kristallstrukturen von [Cp2TiP(SiMe3)2], [(Cp2Ti)2ClAs(SiMe3)2] und [TiCl3 {P(SiMe3)3}2]." Zeitschrift f�r anorganische und allgemeine Chemie 595, no. 1 (April 1991): 57–66. http://dx.doi.org/10.1002/zaac.19915950109.
Повний текст джерелаKunkely, Horst, and Arnd Vogler. "Photoreactivity of Titanocene Pentasulfide." Zeitschrift für Naturforschung B 53, no. 2 (February 1, 1998): 224–26. http://dx.doi.org/10.1515/znb-1998-0214.
Повний текст джерелаKhan, Hina P. A., Dipendu Das, and Tushar Kanti Chakraborty. "Application of Cp2TiCl-Promoted Radical Cyclization: A Unified Strategy for the Syntheses of Iridoid Monoterpenes." Journal of Organic Chemistry 83, no. 11 (May 16, 2018): 6086–92. http://dx.doi.org/10.1021/acs.joc.8b00752.
Повний текст джерелаChakraborty, Tushar Kanti, Rajarshi Samanta, and Sanjib Das. "Radical-Mediated Opening of 2,3-Epoxy Alcohols Using Cp2TiCl: Stereoselective Construction of Quaternary Chiral Centers†." Journal of Organic Chemistry 71, no. 8 (April 2006): 3321–24. http://dx.doi.org/10.1021/jo0600961.
Повний текст джерелаAvdeev, A. V., L. I. Gvinter, and V. Z. Sharf. "Hydrogenation and isomerization of allylbenzene in the presence of the (Cp2TiCl)2-LiAlH4 catalytic system." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 38, no. 3 (March 1989): 655–57. http://dx.doi.org/10.1007/bf00958075.
Повний текст джерелаMonlen, Laura M., Manuel Grande, and Josefa Anaya. "Synthesis of polycyclic ?-lactams. Evolution of tertiary radicals generated by Cp2TiCl from 1,5- and 1,6-epoxynitriles." Tetrahedron 68, no. 52 (December 2012): 10794–805. http://dx.doi.org/10.1016/j.tet.2011.11.015.
Повний текст джерелаAsandei, Alexandru D., Yanhui Chen, Isaac W. Moran, and Gobinda Saha. "Similarities and differences of epoxide, aldehyde and peroxide initiators for Cp2TiCl-catalyzed styrene living radical polymerizations." Journal of Organometallic Chemistry 692, no. 15 (July 2007): 3174–82. http://dx.doi.org/10.1016/j.jorganchem.2007.01.042.
Повний текст джерелаChakraborty, Tushar Kanti, Rajarshi Samanta та Krishnan Ravikumar. "Studies on radical cyclization of 2,3-epoxy alcohols containing a β-(alkoxy)acrylate moiety using Cp2TiCl". Tetrahedron Letters 48, № 36 (вересень 2007): 6389–92. http://dx.doi.org/10.1016/j.tetlet.2007.06.139.
Повний текст джерелаChakraborty, Tushar K., and Sanjib Das. "Synthesis of chiral 1,3-diols by radical-mediated regioselective opening of 2,3-epoxy alcohols using cp2TiCl." Tetrahedron Letters 43, no. 12 (March 2002): 2313–15. http://dx.doi.org/10.1016/s0040-4039(02)00241-1.
Повний текст джерелаBarrero, Alejandro F., M. Mar Herrador, José F. Quílez del Moral, Pilar Arteaga, Jesús F. Arteaga, María Piedra, and Elena M. Sánchez. "Reductive Coupling of Terpenic Allylic Halides Catalyzed by Cp2TiCl: A Short and Efficient Asymmetric Synthesis of Onocerane Triterpenes." Organic Letters 7, no. 12 (June 2005): 2301–4. http://dx.doi.org/10.1021/ol050335r.
Повний текст джерелаLiu, Xiao-hui, Zhong-min Dong, Xiu-lan Tang, and Yue-sheng Li. "Synthesis and characterization of hyperbranched polymers via Cp2TiCl-catalyzed self-condensing vinyl polymerization using glycidyl methacrylate as inimer." Polymer 51, no. 4 (February 2010): 854–59. http://dx.doi.org/10.1016/j.polymer.2009.12.042.
Повний текст джерелаChakraborty, Tushar K., and Sanjib Das. "ChemInform Abstract: Synthesis of Chiral 1,3-Diols by Radical-Mediated Regioselective Opening of 2,3-Epoxy Alcohols Using Cp2TiCl." ChemInform 33, no. 26 (May 21, 2010): no. http://dx.doi.org/10.1002/chin.200226088.
Повний текст джерелаAnaya, Josefa, Manuel Grande, Laura M. Monleón та Ramón M. Sánchez. "Synthesis and reactivity against Cp2TiCl of 4-isoprenyl-β-lactams. Trapping of N-titanoimidoyl radicals from cyanoformyl-2-azetidinones". Tetrahedron 74, № 38 (вересень 2018): 5415–26. http://dx.doi.org/10.1016/j.tet.2018.01.003.
Повний текст джерела