Search results for "ALK"
showing 10 items of 4314 documents
Leaving Group and Regioselectivity Switches in the Aminoalkylation Reaction of Indoles and Related Heterocycles with α-Amido Sulfones
2013
The regioselective aminoalkylation of indoles and related heterocycles with α-amido sulfones under basic conditions has been studied. The reaction that employed the MeMgBr/MgBr2 system provided high yields of 3-(1-carbamoylalkyl)indoles. On the other hand, the reaction that used Cs2CO3 afforded 1-(1-carbamoylalkyl)indoles exclusively in high yields. The first reaction constitutes a switch of the leaving group of the α-amido sulfone in comparison to previously reported reactions between indoles and α-amido sulfones, which provided 3-(1-arylsulfonylalkyl)indoles. The second reaction constitutes a switch in the regioselectivity. The extensions of these C- and N-aminoalkylations starting from p…
N,N-Dimethylformamide Diethyl Acetal
2001
(1; R1 = Et, R2 = Me) [1188-33-6] C7H17NO2 (MW 147.25) InChI = 1S/C7H17NO2/c1-5-9-7(8(3)4)10-6-2/h7H,5-6H2,1-4H3 InChIKey = BWKAYBPLDRWMCJ-UHFFFAOYSA-N (2; R1 = Me, R2 = Me) [4637-24-5] C5H13NO2 (MW 119.19) InChI = 1S/C5H13NO2/c1-6(2)5(7-3)8-4/h5H,1-4H3 InChIKey = ZSXGLVDWWRXATF-UHFFFAOYSA-N (3; R1 = PhCH2, R2 = Me) [2016-04-8] C17H21NO2 (MW 271.39) InChI = 1S/C17H21NO2/c1-18(2)17(19-13-15-9-5-3-6-10-15)20-14-16-11-7-4-8-12-16/h3-12,17H,13-14H2,1-2H3 InChIKey = JFIKHFNGAURIIB-UHFFFAOYSA-N (4; R1 = Et, R2 = Et) [22630-13-3] C9H21NO2 (MW 175.31) InChI = 1S/C9H21NO2/c1-5-10(6-2)9(11-7-3)12-8-4/h9H,5-8H2,1-4H3 InChIKey = AYZXEGOJMRKZCV-UHFFFAOYSA-N (mild and selective reagents for alkylation, f…
Comparative study on the column performance of microparticulate 5-μm C18-bonded and monolithic C18-bonded reversed-phase columns in high-performance …
1999
In this paper we report on the results of a comparative study on the performance of Purospher RP 18e, 5 μm, columns and prototypes of monolithic columns named SilicaROD from Merck, Darmstadt, Germany. The studies were performed on HPLC equipment with minimum extra column contribution. The plate height linear velocity dependency of the Purospher RP 18e column showed a minimum of H of about 10–15 μm at a linear velocity of 1 mm/s. The H versus u curves of the monolithic columns followed the same course. Yet, the curves remained flat up to a linear velocity of about 7 mm/s, where the Purospher RP 18e column could not be operated anymore due to the extremely high back-pressure. In conclusion th…
Über die polykondensation von diäthylphosphit mit aliphastischen diolen
1973
Die Umesterungsreaktion von Diathylphosphit mit linearen Diolen HO–(CH2)x–OH (x = 2–6 und 8) wurde untersucht. Ihre Bilanz zeigte, das neben der angestrebten Umesterungsreaktion in teilweise sehr erheblichem Umfang auch Atherstrukturen gebildet werden. Diese bis jetzt in diesem Zusammenhang noch nicht beschriebene Reaktion verlauft sehr wahrscheinlich im Sinn einer direkten Alkylierung der alkoholischen OH-Gruppen durch die Phosphitestergruppen, denn sie erfordert keinen Katalysator. Die Estergruppen gehen dabei in saure P-OH-Gruppen uber, die unter den angewendeten Bedingungen nicht mehr ohne weiteres zur Kondensation mit den Diolen befahigt sind. Das Verhaltnis von unerwunschter Atherbild…
The Nonanuclear [Mo(IV) {(CN)Fe(III)(3-ethoxy-saldptn)}8]Cl4 Complex Compound Exhibits Multiple Spin Transitions Observed by Mössbauer Spectroscopy
2004
The pentadentate ligand 3-EO-5LH2 = 3-ethoxy-saldptn = N,N′-bis(3-ethoxy-1-hydroxy-2-benzyliden)-1,7-diamino-4-azaheptane has been prepared by a Schiff base condensation between 1,7-diamino-4-azaheptane and the corresponding 3-ethoxy-salicyaldehyde. 3-EO-5LH2 is a sterical extention to 5LH2. Its complexation with Fe(III) gave the high-spin (S = 5/2) complex of [Fe(III)(3-EO-5L)Cl]. This precursor was combined with [Mo(CN)8]4− and a blue nonanuclear cluster [Mo(IV){(CN)Fe(III)(3-EO-5L)}8]Cl4 resulted. This starshaped nonanuclear compound is a high-spin system at room temperature. On cooling to 10 K some of the eight iron(III) centers switched to the low-spin state as proven by Mossbauer spec…
ChemInform Abstract: Cobalt Clusters with Cubane-Type Topologies Based on Trivacant Polyoxometalate Ligands.
2016
Four novel cobalt-substituted polyoxometalates having cobalt cores exhibiting cubane or dicubane topologies have been synthesized and characterized by IR, elemental analysis, electrochemistry, UV–vis spectroscopy, X-ray single-crystal analysis, and magnetic studies. The tetracobalt(II)-substituted polyoxometalate [Co4(OH)3(H2O)6(PW9O34)]4– (1) consists of a trilacunary [B-α-PW9O34]9– unit which accommodates a cubane-like {CoII4O4} core. In the heptacobalt(II,III)-containing polyoxometalates [Co7(OH)6(H2O)6(PW9O34)2]9– (2), [Co7(OH)6(H2O)4(PW9O34)2]n9n– (3), and [Co7(OH)6(H2O)6(P2W15O56)2]15– (4), dicubane-like {CoII6CoIIIO8} cores are encapsulated between two heptadentate [B-α-PW9O34]9– (in…
Microwave-Assisted Synthesis of Polysubstituted 4-Quinolones from Deprotonated α-Aminonitriles
2010
The α-alkylation of deprotonated N-aryl-α-aminonitriles with α-bromoesters furnishes intermediates that can be cyclized to 4-quinolones upon microwave irradiation. Alternatively, base-induced dehydrocyanation of the alkylation products furnishes enaminoesters, which can, for example, be converted into quinoline-3-carboxylates.
ChemInform Abstract: Alkaloid Determination in Crude Extracts from Cortex Quebracho and Opium Applying Capillary Electrophoresis and Capillary Electr…
2010
The applicability of capillary electrophoresis with UV and electrospray ionisation (ESI)-mass spectrometric detection to the determination of alkaloids in crude extracts of Cortex Quebracho and opium has been investigated. The use of a buffer electrolyte consisting of aqueous ammonium acetate (pH 3.1) and acetonitrile resulted in a high performance of peak resolution. Most of the alkaloids have been identified according to the signal of the protonated molecular ion in the ESI mass spectrum
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…
Synthese von 2-alkoxysubstituierten Oligo- und Poly(1,4-phenylenethenylen)en und 2-Arylbenzo[b]furanen mit Hilfe der Siegrist-Reaktion
1994
Synthesis of 2-Alkoxy Substituted Oligo- and Poly(1,4-phenyleneethylene)s and 2-Arylbenzo[b]furanes by Applying the Siegrist Reaction Alkylation of 2-hydroxy-4-methylbenzaldehyde (1) yields the 2-alkoxy-4-methylbenzaldehydes (2a-l) which can be easily transformed to the Schiff bases 3a-l. The intermolecular self-condensation in a strongly alkaline medium leads to the oligo- and poly(1,4-phenyleneethenylene)s (4a-i) with an outstanding regular constitution and overall (E)-configuration. The terminal N-arylamino group can be cleaved by hydrolysis generating the compounds 5a-i. An intramolecular condensation forming the benzo[b]furanes 6j,k is observed for 3j,k – due to the activated OCH2 grou…