Lithium naphthalenide
WebDuring the last three decades, the use of lithium naphthalenide (LN) as a reductant in organic synthesis has increased considerably. It has been used for the reductive cleavage of benzyl ethers, [ ¹ ] N, N, N ′, N ′-tetramethylphosphorodiamidates, [ ² ] and chlorinated aryloxyalkanoic acids. [ ³ ] It was found to be a useful reagent for ... Lithium naphthalene is an organic salt with the chemical formula Li C 10H 8. In the research laboratory, it is used as a reductant in the synthesis of organic, organometallic, and inorganic chemistry. It is usually generated in situ. Lithium naphthalene crystallizes with ligands bound to Li . Meer weergeven The compound is prepared by stirring the metallic lithium with naphthalene in an ethereal solvent, usually as tetrahydrofuran or dimethoxyethane. The resulting salt is dark green. The reaction of naphthalene with lithium … Meer weergeven Redox With a reduction potential near −2.5 V versus the normal hydrogen electrode, the naphthalene radical anion is a strong reducing agent. Meer weergeven Many related radical anions are known such as those derived from anthracene, with other alkali metals (especially sodium), and with diverse ligands attached to the alkali … Meer weergeven
Lithium naphthalenide
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Web23 aug. 1983 · Lithium naphthalenide in THF is becoming an increasingly useful reagent in preparative organolithium chemistry [1-3]. The reagent is prepared from lithium chips and an equivalent amount of naphthalene, and its preparation in synthetically convenient concentrations requires prolonged reaction times, 6-24 h, depending on the stirring … Web15 dec. 2006 · Lithium Naphthalenide Induced Reductive Alkylation of α-Cyano Ketones. A General Method for Regiocontrol of α,α-Dialkylation of Ketones. Reductive Cleavage of …
WebA solution of lithium naphthalenide, a related compound, in tetrahydrofuran. The alkali metal naphthalene salts are prepared by stirring the metal with naphthalene in an … WebMost often lithium and sodium naphthalenide ([LiNaph] and [NaNaph]) were applied and prepared by reacting the respective alkali metal with naphthalene in ethers such as …
WebLithium naphthalenide can be dissolved in ether, benzene, and tetrahydrofuran, and can be stored in solution up to several days. But it must be protected from air and moisture … WebFind lithium naphthalenide and related products for scientific research at MilliporeSigma. US EN. Applications Products Services Support. Advanced Search. Structure Search. Search Within. Products Building Blocks Explorer Technical Documents Site Content Papers Genes Chromatograms. Available for Sale.
Web14 jun. 2016 · The synthesis of the corresponding lithium naphthalenides was performed during 24 h, under continuous and vigorous stirring. Once the synthesis was completed, …
Webmechanism of reaction of geminal dihalides with lithium naphthalenide (linp-center-dot-) - evidence for an electron transfer mechanism - similarities to the mechanism of reaction of geminal dihalides with certain nucleophiles and other one-electron d [j]. ashby ec., deshpande ak. the journal of organic chemistry . 1995,第14期 inb bank of ilWeb陈霄.Synthesis of Intermetallic Pt-Based Catalysts by Lithium Naphthalenide-Driven Reduction for Selective Hydrogenation of Cinnamaldehyde.[J].ACS Applied Materials Interfaces,2024,12(16):18551-18561. inb bank pleasant plains ilWeb29 mrt. 2016 · Metallic titanium (Ti 0) nanoparticles, 1.5 ± 0.4 nm in diameter, are obtained via lithium naphthalenide ( [LiNaph])-driven reduction of TiCl 4 × 2THF in … inb branch interfaceWeb17 okt. 2016 · We have synthesized the products of fluoroethylene carbonate (FEC) and vinylene carbonate (VC) via lithium naphthalenide reduction. By analyzing the resulting … inchoate interest as spouseWebLithium naphthalenide C10H7Li CID 11768624 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and … inchoate in real estateWebPreparation from activated Cb (O).1 An activated Cu, prepared by lithium naphthalenide reduction of CuIPBu3 (12,140), reacts with primary alkyl bromides at -50 to -78° to form alkylcopper reagents that undergo 1,4-addition to cyclo-hexenone in moderate to high yield. This conjugate addition is facilitated by ClSi (CH3)3 and a phosphine. inb bank springfield il wabashWeb15 apr. 2001 · Preparative Methods: anhydrous THF and lithium metal ribbon are cooled to between −40 and −55 °C by use of a 1-hexanol/dry ice bath; 1 … inb business