Bibliografie tematiche / Organobismuth compounds. Catalysis. Ethers

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Letteratura scientifica selezionata sul tema "Organobismuth compounds. Catalysis. Ethers"

Autore: Grafiati
Pubblicato: 4 giugno 2021
Ultima modifica: 1 febbraio 2022

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Articoli di riviste sul tema "Organobismuth compounds. Catalysis. Ethers"

1

Barton, Derek H. R., Jean-Pierre Finet, and Jamal Khamsi. "Copper salts catalysis of N-phenylation of amines by trivalent organobismuth compounds." Tetrahedron Letters 28, no. 8 (1987): 887–90. http://dx.doi.org/10.1016/s0040-4039(01)81015-7.

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2

Narayanaperumal, Senthil, Ricardo S. Schwab, Wystan K. O. Teixeira, and Danilo Yano de Albuquerque. "Recent Advances in the Synthesis of Enantiomerically Enriched Diaryl, Aryl Heteroaryl, and Diheteroaryl Alcohols through Addition of Organometallic Reagents to Carbonyl Compounds." Synthesis 52, no. 13 (2020): 1855–73. http://dx.doi.org/10.1055/s-0039-1690847.

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Abstract (sommario):
Enantiomerically enriched diaryl, aryl heteroaryl, and dihetero­aryl alcohols are an important family of compounds known for their biological properties. Moreover, these molecules are highly privileged scaffolds used as building blocks for the synthesis of pharmaceutically relevant products. This short review provides background on the enantioselective arylation and heteroarylation of carbonyl compounds, as well as, the most significant improvements in this field with special emphasis on the application of organometallic reagents.1 Introduction2 Background on the Enantioselective Synthesis of
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3

Wang, Penghui, Jinying Wang, Chak-Tong Au, Renhua Qiu, Xinhua Xu, and Shuang-Feng Yin. "Air-stable Organobismuth(V) Bisperfluorooctanesulfonate as an Efficient Catalyst for the Synthesis of N-Containing Compounds." Advanced Synthesis & Catalysis 358, no. 8 (2016): 1302–8. http://dx.doi.org/10.1002/adsc.201500998.

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4

Markies, Peter R., Tateo Nomoto, Otto S. Akkerman, Friedrich Bickelhaupt, Wilberth J. J. Smeets, and Anthony L. Spek. "The Activation of Phenylmagnesium Compounds by Crown Ethers." Angewandte Chemie International Edition in English 27, no. 8 (1988): 1084–86. http://dx.doi.org/10.1002/anie.198810841.

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Yamamoto, Yohsuke, Xiang Chen, and Kinya Akiba. "Synthesis and crystal structure of intramolecularly coordinated organobismuth compounds and edge inversion at trivalent bismuth." Journal of the American Chemical Society 114, no. 20 (1992): 7906–7. http://dx.doi.org/10.1021/ja00046a043.

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Katritzky, Alan, Ilhami Celik, and Ashraf Abdel-Fattah. "Thioamidoalkylation of 1,3-Dicarbonyl Compounds, Enol Silyl Ethers, and Enamines." Synthesis 2007, no. 11 (2007): 1655–62. http://dx.doi.org/10.1055/s-2007-966064.

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Nishimura, Norio, Tohru Tanaka, and Takushi Motoyama. "Additivity of the partial molar volumes of organic compounds." Canadian Journal of Chemistry 65, no. 9 (1987): 2248–53. http://dx.doi.org/10.1139/v87-375.

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Abstract (sommario):
A critical test of additivity for partial molar volume has been made at 25 °C in CCl4 with polyethylene glycol dimethyl ethers, crown ethers, cycloalkanes, n-alkanes, and others. Plots of partial molar volume at infinite dilution [Formula: see text] against the properly chosen number of repeating unit (n) are linear except for small cyclic molecules, and the slopes of homologous straight chain and ring compounds are the same. The values of [Formula: see text] extrapolated to n = 0 for cycloalkanes and crown ethers support the validity of the contribution due to the translational kinetic energy
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8

Mpassi, Michel, Gérald Guillaumet, Gérard Coudert, Madeleine Tissier, and Jean Juillard. "Macrocycles polyoxygénés à structure benzodioxinique. Synthèse et étude de la complexation du sodium et du potassium dans le methanol." Canadian Journal of Chemistry 67, no. 7 (1989): 1132–38. http://dx.doi.org/10.1139/v89-170.

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Abstract (sommario):
The synthesis of two new series of polyoxygenated macrocyclic derivatives, 1 and 2, was realised. All these compounds have a 1,4-benzodioxinic moiety and are related to crown ethers, benzocrown ethers, and lariat ethers. The complexing properties of sodium and potassium ions were studied using potentiometry in methanol; results thus obtained are compared to data, previously reported in the literature, for classical polyoxygenated macrocyclic compounds. Keywords: polyoxygenated macrocycles, 1,4-benzodioxin, lariat ethers, sodium and potassium complexes, solvent methanol.
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9

Lyu, Hairong, Ilia Kevlishvili, Xuan Yu, Peng Liu, and Guangbin Dong. "Boron insertion into alkyl ether bonds via zinc/nickel tandem catalysis." Science 372, no. 6538 (2021): 175–82. http://dx.doi.org/10.1126/science.abg5526.

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Abstract (sommario):
Mild methods to cleave the carbon-oxygen (C−O) bond in alkyl ethers could simplify chemical syntheses through the elaboration of these robust, readily available precursors. Here we report that dibromoboranes react with alkyl ethers in the presence of a nickel catalyst and zinc reductant to insert boron into the C−O bond. Subsequent reactivity can effect oxygen-to-nitrogen substitution or one-carbon homologation of cyclic ethers and more broadly streamline preparation of bioactive compounds. Mechanistic studies reveal a cleavage-then-rebound pathway via zinc/nickel tandem catalysis.
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Zhang, Yuhua, and Chao-Jun Li. "Highly Efficient Cross-Dehydrogenative-Coupling between Ethers and Active Methylene Compounds." Angewandte Chemie International Edition 45, no. 12 (2006): 1949–52. http://dx.doi.org/10.1002/anie.200503255.

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Tesi sul tema "Organobismuth compounds. Catalysis. Ethers"

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Speight, Lee Colyer. "Bismuth (III) salt catalyzed cyclic ether syntheses /." 2009. http://hdl.handle.net/10288/1216.

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2

Katkish, Lauren. "Toward biologically active 2,6-disubstituted dihydropyran ring systems using an environmentally benign bismuth catalyst and Mukaiyama aldol reaction /." 2008. http://hdl.handle.net/10288/541.

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Libri sul tema "Organobismuth compounds. Catalysis. Ethers"

1

Bismuthmediated Organic Reactions. Springer, 2012.

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Capitoli di libri sul tema "Organobismuth compounds. Catalysis. Ethers"

1

"14. Introduction of Fluorine with Alkali Metal Fluorides, Including Ammonium Fluoride and Tetraalkylammonium Fluorides (Including Special Methods of Fluorinations, e.g., Phase Transfer Catalysis, Activation by Crown Ethers, Reagents Bound to Polymers)." In Organo-Fluorine Compounds, edited by Baasner, Hagemann, and Tatlow. Georg Thieme Verlag, 1998. http://dx.doi.org/10.1055/b-0035-111166.

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"14. Introduction of Fluorine with Alkali Metal Fluorides, Including Ammonium Fluoride and Tetraalkylammonium Fluorides (Including Special Methods of Fluorinations, e. g., Phase Transfer Catalysis, Activation by Crown Ethers, Reagents Bound to Polymers) : 14.1. With Lithium Fluoride." In Organo-Fluorine Compounds, edited by Baasner, Hagemann, and Tatlow. Georg Thieme Verlag, 1998. http://dx.doi.org/10.1055/b-0035-111167.

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"14. Introduction of Fluorine with Alkali Metal Fluorides, Including Ammonium Fluoride and Tetraalkylammonium Fluorides (Including Special Methods of Fluorinations, e. g., Phase Transfer Catalysis, Activation by Crown Ethers, Reagents Bound to Polymers) : 14.2. With Sodium Fluoride." In Organo-Fluorine Compounds, edited by Baasner, Hagemann, and Tatlow. Georg Thieme Verlag, 1998. http://dx.doi.org/10.1055/b-0035-111168.

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"14. Introduction of Fluorine with Alkali Metal Fluorides, Including Ammonium Fluoride and Tetraalkylammonium Fluorides (Including Special Methods of Fluorinations, e. g., Phase Transfer Catalysis, Activation by Crown Ethers, Reagents Bound to Polymers) : 14.5. Introduction of Fluorine Tetraalkylammonium Fluorides." In Organo-Fluorine Compounds, edited by Baasner, Hagemann, and Tatlow. Georg Thieme Verlag, 1998. http://dx.doi.org/10.1055/b-0035-111172.

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"14. Introduction of Fluorine with Alkali Metal Fluorides, Including Ammonium Fluoride and Tetraalkylammonium Fluorides (Including Special Methods of Fluorinations, e. g., Phase Transfer Catalysis, Activation by Crown Ethers, Reagents Bound to Polymers) : 14.3. With Potassium Fluoride and Potassium Hydrogen Fluoride (I)." In Organo-Fluorine Compounds, edited by Baasner, Hagemann, and Tatlow. Georg Thieme Verlag, 1998. http://dx.doi.org/10.1055/b-0035-111169.

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"14. Introduction of Fluorine with Alkali Metal Fluorides, Including Ammonium Fluoride and Tetraalkylammonium Fluorides (Including Special Methods of Fluorinations, e. g., Phase Transfer Catalysis, Activation by Crown Ethers, Reagents Bound to Polymers) : 14.3. With Potassium Fluoride and Potassium Hydrogen Fluoride (II)." In Organo-Fluorine Compounds, edited by Baasner, Hagemann, and Tatlow. Georg Thieme Verlag, 1998. http://dx.doi.org/10.1055/b-0035-111170.

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"14. Introduction of Fluorine with Alkali Metal Fluorides, Including Ammonium Fluoride and Tetraalkylammonium Fluorides (Including Special Methods of Fluorinations, e. g., Phase Transfer Catalysis, Activation by Crown Ethers, Reagents Bound to Polymers) : 14.4. Introduction of Fluorine with Rubidium and Cesium Fluoride." In Organo-Fluorine Compounds, edited by Baasner, Hagemann, and Tatlow. Georg Thieme Verlag, 1998. http://dx.doi.org/10.1055/b-0035-111171.

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