Search results for " Hydride"
showing 10 items of 43 documents
Bimolecular reduction of 9-alkyl-3-nitrocarbazoles
2007
AbstractReduction of 9-alkyl-3-nitrocarbazoles (Ia–Ie) with lithium aluminium hydride gave corresponding 9,9′-dialkyl-3,3′-azocarbazoles (IIa–IIe) in moderate yield. By the action of zinc dust in alcohol and aqueous alkali on I or II, 5,13-dialkyldiindolo[3,2-a,d]phenazines (IIIa–IIId) were obtained. Parent compounds, viz. 3,3′-azocarbazole (IIf) and diindolo[3,2-a,d]phenazine (IIIf) could not be obtained in these ways. Compound IIf was obtained in Vorländer reaction and IIIf by thermal decomposition of 3-azidocarbazole. Formation of IIIa–IIId is explained as a result of ortho-benzidine rearrangement of hypothetical 9,9′-dialkyl-3,3′-hydrazocarbazoles.
2020
Reduction of the aluminum iodide AlI2AriPr8 (1; AriPr8 = C6H-2,6-(C6H2-2,4,6-Pri3)2-3,5-Pri2) with 5% w/w Na/NaCl in hexanes gave a dark red solution from which the monomeric alanediyl :AlAriPr8 (2) was isolated in ca. 28% yield as yellow-orange crystals. Compounds 1 and 2 were characterized by X-ray crystallography, electronic and NMR spectroscopy, and theoretical calculations. The Al atom in 2 is one-coordinate, and the compound displays two absorptions in its electronic spectrum at 354 and 455 nm. It reacts with H2 under ambient conditions to give the aluminum hydride {AlH(μ-H)AriPr8}2, probably via a weakly bound dimer of 2 as an intermediate.
Carbazole synthesisviaanin situtrapping strategy with indolyl enol ethers
1994
Indolyl enol ethers, generated from the alkoxy(indolyl)carbenium tetra- fluoroborates (1) by treatment with sodium hydride, can be trapped with dimethyl acetylenedicarboxylate or N-phenylmaleimide to furnish the se- lectively functionalized carbazoles (3), (4), (5), (9), (10), and (13). In addition, the biaryl derivatives (6) and (11) are produced by a ring- opening reaction of the primarily formed Diels-Alder adduct. In the case of the biaryl derivative (6), an X-ray crystal structure analysis yields valuable information on constitutions and configurations in the biaryl series. The phenomenon of atropisomerism is discussed for this compound
Über die reduktion von polyacrylsäurederivaten
1960
Bei der Reduktion von Polyacrylsaurechlorid und von Polyacrylsaure-N-methylanilid mit Lithiumaluminium-tri-tert.-butoxyhydrid bzw. Lithiumaluminiumhydrid entstehen Polymere mit 30–50 Mol-% Aldehydgruppen. Aus Polyacrylsaurechloriden, Polyacrylsauremethylestern und Polyacroleinen wurden bei der Reduktion mit Lithiumaluminiumhydrid bzw. Kaliumborhydrid identische polymere Allylalkohole erhalten. Diese lassen sich acylieren, tritylieren und tosylieren. Die Polyallyl- und Polyvinyl-dinitrobenzoate bilden mit α-Naphthylamin und Benzidin gefaurbte Molekulverbindungen. The reduction of polyacrylyl chloride and polyacryl-N-methylanilide with lithium aluminum tri-tert-butoxyhydride and lithium alumi…
Chemoenzymatische „Chiral-Pool”-Synthese von (+)-exo-Brevicomin aus Kohlenhydraten mit Fructose-1,6-diphosphat-Aldolase
1990
Chemoenzymatic “Chiral-Pool” Synthesis of (+)-exo-Brevicomin from Carbohydrates Using Fructose 1,6-Diphosphate Aldolase Fructose-1,6-diphosphate aldolase (EC 4.1.2.13) catalyzes the stereospecific aldol reaction between 1,3-dihydroxyacetone phosphate (4) and 5-oxohexanal (3) or its 5-dithiane-protected analog 8. The products of the aldol reactions are dephosphorylated with acid phosphatase (EC 3.1.3.2). Whereas the aldol adduct of 3 cyclizes spontaneously to give the bicyclic brevicomin precursor 3, the adduct of 8 first has to be deprotected with sulfuryl chloride and wet silica gel. The resulting bicyclic α-hydroxy ketone 3 is reduced with LiAlH4 to form the 1,2-diol 14 which is then deox…
Pencil Lead as a Matrix for MALDI-ToF Mass Spectrometry of Sensitive Functional Polymers
2007
With the increase in complexity of functional polymers in recent years, MALDI-ToF has become an important tool for gaining precise information on polymer functionality, end groups, and, in special cases, molecular weights. Here we describe how pencil lead, deposited by simply drawing with a regular pencil onto conventional MALDI-ToF targets, can be used as a very attractive matrix for MALDI-ToF mass spectrometry of synthetic polymers. Highly sensitive polymers such as silyl hydride functional poly(styrene), poly(butadiene), and poly(isoprene) have been investigated using conventional MALDI-ToF matrices as well as pencil lead. In all cases, the use of pencil lead prevented oxidation of the h…
Alkylumlagerungen und acidolyse der ethylidenbrücken bei der synthese von ethylidendiphenolen
1990
For the synthesis of symmetrical and unsymmetrical ethylidenediphenols the corresponding hydroxyphenylethanols (1a–c) were prepared by hydrogenation of hydroxyphenyl methyl ketones with hydrogen/Raney nickle or with lithium aluminium hydride. Condensations of the hydroxyphenylethanols with different phenols under the usual acidic conditions gave products formally resulting form transalkylations. Only the reaction of 1-(3-bromo-2-hydroxy-5-methylphenyl)ethanol (1c) with p-cresol gave the expected product 2d with 82% yield. Experiments with ethylidenediphenols showed that with acids in presence or absence of phenols cleavage and recondensations take place leading to products of formal transal…
SYNTHESIS AND REARRANGEMENT OFN-METHYL-N-(2-THIAZOLYL)-NITRAMINE
2001
Methylation of N-(2-thiazolyl)-nitramine in alkaline solution gives 1,2-dihydro-3-methyl-2-nitriminothiazole which rear-ranges in concentrated sulphuric acid yielding small amount of 2-(N-methylamino)-5-nitrothiazole, identical with the product of rearrangement of N-methyl-N-(2-thiazolyl)-nitramine. The latter compound was obtained by the action of sodium hydride on 2-(N-methylamino)-thiazole followed by the nitration with n-butyl nitrate.
Combinatorial Identification of Hydrides in a Ligated Ag40 Nanocluster with Non-compact Metal Core
2019
No formation of bulk silver hydride has been reported. Until very recently, only few silver nanoclusters containing hydrides have been successfully prepared. However, due to the lack of effective techniques and also poor stability of hydride-containing Ag nanoclusters, the identification of hydrides’ location within Ag nanoclusters is challenging and not yet achieved although some successes have been reported on clusters of several Ag atoms. In this work, we report a detailed structural and spectroscopic characterization of the [Ag40(DMBT)24(PPh3)8H12]2+ (Ag40H12) cluster (DMBT=2,4-dimethylbenzenethiol). The metal framework consists of three-concentric shells of Ag8@Ag24@Ag8 which can be de…