Search results for "Silver salts"
showing 4 items of 4 documents
[Bis(phosphonio)isophosphindolide]silver complexes
1996
The outcome of reactions of bis(phosphonio)isophosphindolide salts 1[X] and 6[X] (X- Cl-, Br-, CF3SO3-) with silver salts AgY (Y- = CF3SO3-, CF3CO2-, CH3CO2-, 1/2 SO4-) depends strongly on the available anions X, Y. If X-, Y- CF3SO3-, both mononuclear and dinuclear silver complexes are formed which exhibit either μ1,μ1(P) or μ2,η1(P) coordination of the cations 1, 6 to one or to both metals. In solution, dynamic equilibria between both types of products and free 1, 6 were detected by 31P-NMR spectroscopy. Mononuclear (4a, 7) and dinuclear (5a, 8) complexes were isolated as solvates with CHCl3 or THF. If X-, Y- = CF3CO2, only equilibrium mixtures between the free ligands and silver complexes…
Synthesis of Dienedioic and Tetraenedioic Acids by Oxidative Coupling of Unsaturated Carboxylic Acid Dienediolates by 1,2-Diiodoethane
1993
Abstract Acyclic and cyclic unsaturated carboxylic acids 1 to 4 are most easily converted to unsaturated dicarboxylic acids 5 to 8 by oxidative coupling of their diene- or triene-diolates by 1,2-diiodoethane. This procedure improves formerly reported oxidations by iodine or silver salts.
ChemInform Abstract: Synthesis of Dienedioic and Tetraenedioic Acids by Oxidative Coupling of Unsaturated Carboxylic Acid Dienediolates by 1,2-Diiodo…
2010
Abstract Acyclic and cyclic unsaturated carboxylic acids 1 to 4 are most easily converted to unsaturated dicarboxylic acids 5 to 8 by oxidative coupling of their diene- or triene-diolates by 1,2-diiodoethane. This procedure improves formerly reported oxidations by iodine or silver salts.
Glycosidsynthese mit 2,3,4,6-Tetra-O-pivaloyl-α-D-glucopyrancsylbromid
1982
Die Glycosylierung von Benzylalkohol und Cholesterin gelingt mit 2,3,4,6-Tetra-O-pivaloyl-α-D-glucopyranosylbromid (2) in Gegenwart von Silbersalzen in hoher Ausbeute. Die bei Koenigs-Knorr-Synthesen mit 2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosylbromid (5) storende Orthoesterbildung wird beim Einsatz von 2 weitgehend unterdruckt. Die Lenkung der Reaktion zugunsten der Glycosidbildung wird dadurch erklart, das der tert-Butyl-Substituent im zwischenzeitlich gebildeten Acyloxoniumion A den nucleophilen Angriff am Acyloxoniumkohlenstoff sterisch behindert. Glycoside Synthesis Using 2,3,4,6-Tetra-O-pivaloyl-α-D-glucopyranosyl Bromide In the presence of silver salts the glycosylation of benzyl alc…