The Sonogashira cross-coupling of 4,6-dichloro-2-pyrone with terminal acetylenes proceeds in good yields and high regioselectivity for the 6-position; dibenzylidene acetone (dba) type ligands play a non-innocent role in reactions mediated by Pd(dba)(2)/PPh3; theoretical studies indicate that C-6 oxidative addition is favoured both kinetically and thermodynamically
The Sonogashira reaction is a cross-coupling reaction of a vinyl or aryl halide with a terminal alky...
In this thesis work, an extensive study was carried out on the synthesis of alkynes via Pd-catalyzed...
An operationally simple approach for the regioselective tandem synthesis of indolo[1,2-<i>a</i>]qu...
The mechanism of the copper-free Sonogashira cross-coupling was investigated using a model reaction ...
The coupling of aryl or vinyl halides with terminal acetylenes catalysed by palladium, commonly kno...
The conversion–time data for 168 different Pd/Cu-catalyzed Sonogashira cross-coupling reactions of f...
The Sonogashira cross-coupling reaction involves the coupling of terminal alkynes with aryl or vinyl...
The Sonogashira cross-coupling reaction is the most frequently employed synthetic procedure for the ...
The incorporation of alkynes into organic molecules is one of the most valuable transformations for ...
An unreported product outcome from an intended Sonogashira coupling is presented. The generality of ...
p-Bromo- or p-iodophenylthioacetate can react with trimethylsilylacetylene by simultaneous Sonogashi...
Unsymmetrical diarylalkynes have attracted much atten-tion, as the molecule structure, having an int...
Horstmann J, Reger S, Neumann B, Stammler H-G, Mitzel NW. One-pot desilylation-Sonogashira coupling....
The acyl Sonogashira reaction represents an extension of Sonogashira cross-coupling to acid chloride...
International audienceThe Sonogashira cross-coupling reaction is the most useful tool for the format...
The Sonogashira reaction is a cross-coupling reaction of a vinyl or aryl halide with a terminal alky...
In this thesis work, an extensive study was carried out on the synthesis of alkynes via Pd-catalyzed...
An operationally simple approach for the regioselective tandem synthesis of indolo[1,2-<i>a</i>]qu...
The mechanism of the copper-free Sonogashira cross-coupling was investigated using a model reaction ...
The coupling of aryl or vinyl halides with terminal acetylenes catalysed by palladium, commonly kno...
The conversion–time data for 168 different Pd/Cu-catalyzed Sonogashira cross-coupling reactions of f...
The Sonogashira cross-coupling reaction involves the coupling of terminal alkynes with aryl or vinyl...
The Sonogashira cross-coupling reaction is the most frequently employed synthetic procedure for the ...
The incorporation of alkynes into organic molecules is one of the most valuable transformations for ...
An unreported product outcome from an intended Sonogashira coupling is presented. The generality of ...
p-Bromo- or p-iodophenylthioacetate can react with trimethylsilylacetylene by simultaneous Sonogashi...
Unsymmetrical diarylalkynes have attracted much atten-tion, as the molecule structure, having an int...
Horstmann J, Reger S, Neumann B, Stammler H-G, Mitzel NW. One-pot desilylation-Sonogashira coupling....
The acyl Sonogashira reaction represents an extension of Sonogashira cross-coupling to acid chloride...
International audienceThe Sonogashira cross-coupling reaction is the most useful tool for the format...
The Sonogashira reaction is a cross-coupling reaction of a vinyl or aryl halide with a terminal alky...
In this thesis work, an extensive study was carried out on the synthesis of alkynes via Pd-catalyzed...
An operationally simple approach for the regioselective tandem synthesis of indolo[1,2-<i>a</i>]qu...
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