Статті в журналах з теми "Aluminium(I) Nucleophile"
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Hinz, Alexander, and Frank Breher. "An Anionic Aluminium Nucleophile." Angewandte Chemie International Edition 57, no. 29 (June 14, 2018): 8818–20. http://dx.doi.org/10.1002/anie.201804930.
Повний текст джерелаNishi, Takafumi, Isao Mizota, and Makoto Shimizu. "Integrated reactions using addition to conjugated imines and iminium salts." Pure and Applied Chemistry 84, no. 12 (June 30, 2012): 2609–17. http://dx.doi.org/10.1351/pac-con-12-01-03.
Повний текст джерелаZhang, Zhichao, Tianming Wang, Peng Xiang, Qinqin Du, and Shuang Han. "Syntheses, Characterization, and Application of Tridentate Phenoxyimino-Phenoxy Aluminum Complexes for the Coupling of Terminal Epoxide with CO2: From Binary System to Single Component Catalyst." Catalysts 11, no. 2 (January 20, 2021): 145. http://dx.doi.org/10.3390/catal11020145.
Повний текст джерелаCheng, Xu, Shuchen Pei, Chenchen Xue, Kaifei Cao, Li Hai та Yong Wu. "Reactions of β-diketone compounds with nitriles catalyzed by Lewis acids: a simple approach to β-enaminone synthesis". RSC Adv. 4, № 109 (2014): 63897–900. http://dx.doi.org/10.1039/c4ra10879e.
Повний текст джерелаKonshin, Valery V., Vitaly A. Shcherbinin, Ida A. Lupanova, and Dzhamilya N. Konshina. "Aluminum Triflate—Catalyzed Adamantylation of N-Nucleophiles." Proceedings 9, no. 1 (November 14, 2018): 21. http://dx.doi.org/10.3390/ecsoc-22-05661.
Повний текст джерелаYamashita, Makoto. "Characteristic Reactions of Nucleophilic Aluminum Anion." Journal of Synthetic Organic Chemistry, Japan 79, no. 5 (May 1, 2021): 457–64. http://dx.doi.org/10.5059/yukigoseikyokaishi.79.457.
Повний текст джерелаRanishenka, B. V., I. A. Chelnokova, and A. A. Poznyak. "Aluminium and mica azide surface functionalization." Proceedings of the National Academy of Sciences of Belarus, Chemical Series 58, no. 4 (November 29, 2022): 379–86. http://dx.doi.org/10.29235/1561-8331-2022-58-4-379-386.
Повний текст джерелаEsrafili, Mehdi D. "A DFT study on electronic structure and local reactivity descriptors of pristine and carbon-substituted AlN nanotubes." Canadian Journal of Chemistry 91, no. 8 (August 2013): 711–17. http://dx.doi.org/10.1139/cjc-2013-0103.
Повний текст джерелаCullen, Adam, Alfred J. Muller, and D. Bradley G. Williams. "Protecting group-free use of alcohols as carbon electrophiles in atom efficient aluminium triflate-catalysed dehydrative nucleophilic displacement reactions." RSC Advances 7, no. 67 (2017): 42168–71. http://dx.doi.org/10.1039/c7ra08784e.
Повний текст джерелаKasal, Alexander, and Jaroslav Zajíček. "Solvolysis of Westphalen-type compounds." Collection of Czechoslovak Chemical Communications 51, no. 7 (1986): 1462–75. http://dx.doi.org/10.1135/cccc19861462.
Повний текст джерелаVeselý, Ivan, and Václav Dědek. "Reactivity of 2,2-difluoro-3-methyl-3-butenal toward some O-, N- and C-nucleophiles." Collection of Czechoslovak Chemical Communications 50, no. 12 (1985): 2730–42. http://dx.doi.org/10.1135/cccc19852730.
Повний текст джерелаMesías-Salazar, Ángela, Yersica Rios Yepes, Javier Martínez, and René S. Rojas. "Highly Active CO2 Fixation into Cyclic Carbonates Catalyzed by Tetranuclear Aluminum Benzodiimidazole-Diylidene Adducts." Catalysts 11, no. 1 (December 22, 2020): 2. http://dx.doi.org/10.3390/catal11010002.
Повний текст джерелаDeora, Nipa, and Paul R. Carlier. "A computational study of regioselectivity in aluminum hydride ring-opening of cis- and trans-4-t-butyl and 3-methylcyclohexene oxides." Organic & Biomolecular Chemistry 17, no. 37 (2019): 8628–35. http://dx.doi.org/10.1039/c9ob01675a.
Повний текст джерелаWong, C. M., P. M. Gordon, A. G. Chen, and H. Y. P. Lam. "The total synthesis of (±)-4-demethoxy-10-nordaunomycinone." Canadian Journal of Chemistry 65, no. 6 (June 1, 1987): 1375–79. http://dx.doi.org/10.1139/v87-232.
Повний текст джерелаErb, William, Florence Mongin, Nahida Brikci-Nigassa, and Ghenia Bentabed-Ababsa. "In Situ ‘Trans-Metal Trapping’: An Efficient Way to Extend the Scope of Aromatic Deprotometalation." Synthesis 50, no. 18 (March 8, 2018): 3615–33. http://dx.doi.org/10.1055/s-0036-1591953.
Повний текст джерелаSaito, Susumu, Toshihiko Sone, Masaaki Murase, and Hisashi Yamamoto. "Aluminum Tris(2,6-diphenylphenoxide)-ArCOCl Complex for Nucleophilic Dearomatic Functionalization." Journal of the American Chemical Society 122, no. 41 (October 2000): 10216–17. http://dx.doi.org/10.1021/ja0014382.
Повний текст джерелаHarder, Sjoerd, and Jan Spielmann. "Unprecedented reactivity of an aluminium hydride complex with ArNH2BH3: nucleophilic substitution versus deprotonation." Chemical Communications 47, no. 43 (2011): 11945. http://dx.doi.org/10.1039/c1cc14689k.
Повний текст джерелаSaito, Susumu, Toshihiko Sone, Masaaki Murase, and Hisashi Yamamoto. "ChemInform Abstract: Aluminum Tris(2,6-diphenylphenoxide)-ArCOCl Complex for Nucleophilic Dearomatic Functionalization." ChemInform 32, no. 7 (May 30, 2010): no. http://dx.doi.org/10.1002/chin.200107075.
Повний текст джерелаSudhakar, Kolanu, Atif Mahammed, Natalia Fridman, and Zeev Gross. "Iodinated cobalt corroles." Journal of Porphyrins and Phthalocyanines 21, no. 12 (December 2017): 900–907. http://dx.doi.org/10.1142/s108842461750095x.
Повний текст джерелаColby, David, Francis Barrios, Brannon Springer, and Robert Hazlitt. "Effect of Substituents and Stability of Transient Aluminum–Aminals in the Presence of Nucleophiles." Synthesis 47, no. 02 (December 5, 2014): 175–80. http://dx.doi.org/10.1055/s-0034-1379635.
Повний текст джерелаEl-Samahy, Fatma A. "A stereochemical investigation of the nucleophilic addition of methyl ethyl ketone to (E)-alkyloxindolylideneacetates." Journal of Chemical Research 2005, no. 1 (January 2005): 62–66. http://dx.doi.org/10.3184/0308234053431031.
Повний текст джерелаEisch, John J. "Emergence of electrophilic alumination as the counterpart of established nucleophilic lithiation: an academic sojourn in organometallics with William Kaska as fellow traveler." Dalton Transactions 44, no. 15 (2015): 6671–79. http://dx.doi.org/10.1039/c4dt01036a.
Повний текст джерелаMercer, Frank W. "Synthesis and Properties of Aromatic Poly(Ether Ketone Pyridazine)s." High Performance Polymers 5, no. 4 (August 1993): 275–83. http://dx.doi.org/10.1088/0954-0083/5/4/002.
Повний текст джерелаWang, Kang-Kyun, Bong-Jin Kim, Si-Hwan Ko, Dong Hoon Choi, and Yong-Rok Kim. "Fabrication of Photofunctional Nanoporous Membrane and Its Photoinactivation Effect of Vesicular Stomatitis Virus." Journal of Nanomaterials 2012 (2012): 1–7. http://dx.doi.org/10.1155/2012/454507.
Повний текст джерелаZhang, Zaihui, T. L. Thomas Hui, and Chris Orvig. "One-pot synthesis of N-substituted-3-hydroxy-4-pyridinone chelate complexes of aluminum, gallium, and indium." Canadian Journal of Chemistry 67, no. 11 (November 1, 1989): 1708–10. http://dx.doi.org/10.1139/v89-263.
Повний текст джерелаShimizu, Makoto, Chiaki Yamauchi та Toshiki Ogawa. "Double Nucleophilic Addition of Azide and Tetramethallyltin to α,β-Unsaturated Aldimines Promoted by Aluminum Chloride". Chemistry Letters 33, № 5 (травень 2004): 606–7. http://dx.doi.org/10.1246/cl.2004.606.
Повний текст джерелаPower, Michael B., Andrew R. Barron, Simon G. Bott, and Jerry L. Atwood. ".pi.-Face selectivity of coordinated ketones to nucleophilic additions: the importance of aluminum-oxygen .pi.-bonding." Journal of the American Chemical Society 112, no. 9 (April 1990): 3446–51. http://dx.doi.org/10.1021/ja00165a031.
Повний текст джерелаTian, Guocai, Huanhuan Du, and Hongmei Zhang. "First Principle Analysis on Pyridine Amide Derivatives’ Adsorption Behavior on the Pt (111) Surface." Crystals 11, no. 2 (January 24, 2021): 98. http://dx.doi.org/10.3390/cryst11020098.
Повний текст джерелаBARRIUSO, E., J. M. PORTAL, and F. ANDREUX. "CINÉTIQUE ET MÉCANISME DE L'HYDROLYSE ACIDE DE LA MATIÈRE ORGANIQUE D'UN SOL HUMIFÈRE DE MONTAGNE." Canadian Journal of Soil Science 67, no. 3 (August 1, 1987): 647–58. http://dx.doi.org/10.4141/cjss87-061.
Повний текст джерелаMaruoka, Keiji, Masahiro Ito, and Hisashi Yamamoto. "Unprecedented nucleophilic addition of organolithiums to aromatic aldehydes and ketones by complexation with aluminum tris(2,6-diphenylphenoxide)." Journal of the American Chemical Society 117, no. 35 (September 1995): 9091–92. http://dx.doi.org/10.1021/ja00140a036.
Повний текст джерелаMorse, Graham E., and Timothy P. Bender. "Aluminum Chloride Activation of Chloro-Boronsubphthalocyanine: a Rapid and Flexible Method for Axial Functionalization with an Expanded Set of Nucleophiles." Inorganic Chemistry 51, no. 12 (May 29, 2012): 6460–67. http://dx.doi.org/10.1021/ic2016935.
Повний текст джерелаBaer, Hans H., and Miroslawa Mekarska-Falicki. "Stereochemical dependence of the mechanism of deoxygenation, with lithium triethylborohydride, in 4,6-O-benzylidenehexopyranoside p-toluenesulfonates." Canadian Journal of Chemistry 63, no. 11 (November 1, 1985): 3043–52. http://dx.doi.org/10.1139/v85-505.
Повний текст джерелаShimizu, Makoto, Toshiki Ogawa та Takafumi Nishi. "Double nucleophilic addition reaction to α,β-unsaturated aldimines promoted by aluminum chloride and a limited amount of water". Tetrahedron Letters 42, № 32 (серпень 2001): 5463–66. http://dx.doi.org/10.1016/s0040-4039(01)01021-8.
Повний текст джерелаShimizu, Makoto, Makiko Kamiya та Iwao Hachiya. "Double Nucleophilic Addition of Trimethylsilyl Cyanide to α,β-Unsaturated Aldimines Promoted by Aluminum Chloride: Preparation of 2-Aminopentanedinitrile". Chemistry Letters 34, № 10 (жовтень 2005): 1456–57. http://dx.doi.org/10.1246/cl.2005.1456.
Повний текст джерелаMARUOKA, K., M. ITO, and H. YAMAMOTO. "ChemInform Abstract: Unprecedented Nucleophilic Addition of Organolithiums to Aromatic Aldehydes and Ketones by Complexation with Aluminum Tris(2,6- diphenylphenoxide)." ChemInform 26, no. 52 (August 13, 2010): no. http://dx.doi.org/10.1002/chin.199552052.
Повний текст джерелаSugimoto, Hiroshi, Takuzo Aida, and Shohei Inoue. "Lewis acid-promoted living anionic polymerization of alkyl methacrylates initiated with aluminum porphyrins. Importance of steric balance between a nucleophile and a Lewis acid." Macromolecules 27, no. 13 (June 1994): 3672–74. http://dx.doi.org/10.1021/ma00091a033.
Повний текст джерелаDmowski, Wojciech. "Nucleophilic reactions of fluoroolefins. VI. Reactions of 1-phenylpentafluoropropene with lithium aluminium hydride. Regio- and stereoselective substitution of vinylic fluorines by hydrogen." Journal of Fluorine Chemistry 29, no. 3 (September 1985): 273–86. http://dx.doi.org/10.1016/s0022-1139(00)82327-1.
Повний текст джерелаShimizu, Makoto, Makiko Kamiya та Iwao Hachiya. "Double Nucleophilic Addition of Ketene Silyl (Thio)acetals and Trimethylsilyl Cyanide to α,β-Unsaturated Aldimines Promoted by Aluminum Chloride". Chemistry Letters 32, № 7 (липень 2003): 606–7. http://dx.doi.org/10.1246/cl.2003.606.
Повний текст джерелаTakeda, Norihiko, Erika Futaki, Yukiko Kobori, Masafumi Ueda та Okiko Miyata. "Nucleophilic Arylation of N ,O -Ketene Acetals with Triaryl Aluminum Reagents: Access to α-Aryl Amides through an Umpolung Process". Angewandte Chemie International Edition 56, № 51 (27 листопада 2017): 16342–46. http://dx.doi.org/10.1002/anie.201708665.
Повний текст джерелаTakeda, Norihiko, Erika Futaki, Yukiko Kobori, Masafumi Ueda та Okiko Miyata. "Nucleophilic Arylation of N ,O -Ketene Acetals with Triaryl Aluminum Reagents: Access to α-Aryl Amides through an Umpolung Process". Angewandte Chemie 129, № 51 (27 листопада 2017): 16560–64. http://dx.doi.org/10.1002/ange.201708665.
Повний текст джерелаKuroki, Masakatsu, Tsuyoshi Watanabe, Takuzo Aida, and Shohei Inoue. "Steric separation of nucleophile and Lewis acid providing dramatically accelerated reaction. High-speed polymerization of methyl methacrylate with enolate-aluminum porphyrin/sterically crowded organoaluminum systems." Journal of the American Chemical Society 113, no. 15 (July 1991): 5903–4. http://dx.doi.org/10.1021/ja00015a077.
Повний текст джерелаRamsden, Nigel G., George W. J. Fleet, and Sung Keon Namgoong. "Interception of an iminium ion equivalent by intramolecular nucleophilic attack by a silyl ether during lithium aluminium hydride reduction of a tertiary lactam." Journal of the Chemical Society, Perkin Transactions 2, no. 12 (1991): 1991. http://dx.doi.org/10.1039/p29910001991.
Повний текст джерелаOlah, George A., Imre Bucsi, Christian Lambert, Robert Aniszfeld, Nirupam J. Trivedi, Dilip K. Sensharma, and G. K. Surya Prakash. "Chlorination and bromination of fullerenes. Nucleophilic methoxylation of polychlorofullerenes and their aluminum trichloride catalyzed Friedel-Crafts reaction with aromatics to polyarylfullerenes." Journal of the American Chemical Society 113, no. 24 (November 1991): 9385–87. http://dx.doi.org/10.1021/ja00024a063.
Повний текст джерелаPark, Seung Un, Sung Kee Chung, and Martin Newcomb. "Evidence supporting two-electron nucleophilic displacement in reactions of unhindered alkyl bromides and iodides with boron and aluminum hydride reducing agents." Journal of Organic Chemistry 52, no. 15 (July 1987): 3275–78. http://dx.doi.org/10.1021/jo00391a017.
Повний текст джерелаShimizu, Makoto, Toshiki Ogawa та Takafumi Nishi. "ChemInform Abstract: Double Nucleophilic Addition Reaction to α,β-Unsaturated Aldimines Promoted by Aluminum Chloride and a Limited Amount of Water." ChemInform 32, № 43 (24 травня 2010): no. http://dx.doi.org/10.1002/chin.200143075.
Повний текст джерелаReheim, Mohamed A. M. A., Ibrahim S. A. Hafiz, and Hend S. E. A. Rady. "Utility of Diketone in Heterocyclic Synthesis: Synthesis of New Substituted Pyrimidines and Fused Pyrimidine of Potential Biosignificant Interest." Current Organic Synthesis 15, no. 8 (December 17, 2018): 1171–81. http://dx.doi.org/10.2174/1570179415666180918161101.
Повний текст джерелаNayl, AbdElAziz A., Ashraf A. Aly, Wael A. A. Arafa, Ismail M. Ahmed, Ahmed I. Abd-Elhamid, Esmail M. El-Fakharany, Mohamed A. Abdelgawad, Hendawy N. Tawfeek, and Stefan Bräse. "Azides in the Synthesis of Various Heterocycles." Molecules 27, no. 12 (June 9, 2022): 3716. http://dx.doi.org/10.3390/molecules27123716.
Повний текст джерелаHirabe, Tomoatsu, Masato Takagi, Kiyoshige Muraoka, Masatomo Nojima, and Shigekazu Kusabayashi. "Lithium aluminum hydride reduction of 1-aryl-3-halopropenes, 1-aryl-3-halobutenes, and (9-anthryl)arylmethyl halides. Nucleophilic substitution vs. single electron transfer." Journal of Organic Chemistry 50, no. 11 (May 1985): 1797–802. http://dx.doi.org/10.1021/jo00211a002.
Повний текст джерелаRAMSDEN, N. G., G. W. J. FLEET, and S. K. NAMGOONG. "ChemInform Abstract: Interception of an Iminium Ion Equivalent by Intramolecular Nucleophilic Attack by a Silyl Ether During Lithium Aluminum Hydride Reduction of a Tertiary Lactam." ChemInform 23, no. 13 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199213302.
Повний текст джерелаViñals, F., X. Testar, M. Palacín, and A. Zorzano. "Inhibitory effect of fluoride on insulin receptor autophosphorylation and tyrosine kinase activity." Biochemical Journal 291, no. 2 (April 15, 1993): 615–22. http://dx.doi.org/10.1042/bj2910615.
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