The Sonogashira cross-coupling reaction is the most frequently employed synthetic procedure for the preparation of arylated alkynes, which are important conjugated compounds with multiple applications. Despite of their rather high price, this reaction is usually catalyzed by palladium species, making the recovery and reuse of the catalyst an interesting topic, mainly for industrial purposes. Easy recycle can be achieved anchoring the palladium catalyst to a separable support. This review shows recent developments in the use of palladium species anchored to different solid supports as recoverable catalysts for Sonogashira cross-coupling reactions
A novel supported catalyst formed by an oxime-derived palladacycle supported on clay OxPdCy@clay is ...
An MCM-48 supported 2-pyridinylmethanimine Pd-catalyst was found to be a highly efficient catalyst i...
The Pd–Cu catalysed Sonogashira coupling of terminal alkynes and aryl halides is a cornerstone synth...
The Sonogashira cross-coupling reaction is the most frequently employed synthetic procedure for the ...
The development of new solid supports for palladium has received a lot of interest lately. These cat...
The development of new solid supports for palladium has received a lot of interest lately. These cat...
The Sonogashira cross coupling of aryl iodides with terminal alkynes has been carried out in the pre...
The commercially available and cheap Pd/C was found to promote Sonogashira couplings in the environm...
A heterogeneous catalyst, nanosized MCM-41-Pd, was used to catalyze the Sonogashira coupling of aryl...
A new family of well-defined NHC-Pd complexes immobilised onto silica, alumina and titania is report...
Sonogashira reaction and oxidative dimerisation of terminal alkynes are among the most relevant and ...
*Talat, Baran ( Aksaray, Yazar )Palladium (Pd) complexes supported on the polymers have been widely ...
The Sonogashira reaction, a palladium catalyzed cross-coupling reaction, was performe
The Sonogashira cross-coupling reaction involves the coupling of terminal alkynes with aryl or vinyl...
The Sonogashira reaction is a cross-coupling reaction of a vinyl or aryl halide with a terminal alky...
A novel supported catalyst formed by an oxime-derived palladacycle supported on clay OxPdCy@clay is ...
An MCM-48 supported 2-pyridinylmethanimine Pd-catalyst was found to be a highly efficient catalyst i...
The Pd–Cu catalysed Sonogashira coupling of terminal alkynes and aryl halides is a cornerstone synth...
The Sonogashira cross-coupling reaction is the most frequently employed synthetic procedure for the ...
The development of new solid supports for palladium has received a lot of interest lately. These cat...
The development of new solid supports for palladium has received a lot of interest lately. These cat...
The Sonogashira cross coupling of aryl iodides with terminal alkynes has been carried out in the pre...
The commercially available and cheap Pd/C was found to promote Sonogashira couplings in the environm...
A heterogeneous catalyst, nanosized MCM-41-Pd, was used to catalyze the Sonogashira coupling of aryl...
A new family of well-defined NHC-Pd complexes immobilised onto silica, alumina and titania is report...
Sonogashira reaction and oxidative dimerisation of terminal alkynes are among the most relevant and ...
*Talat, Baran ( Aksaray, Yazar )Palladium (Pd) complexes supported on the polymers have been widely ...
The Sonogashira reaction, a palladium catalyzed cross-coupling reaction, was performe
The Sonogashira cross-coupling reaction involves the coupling of terminal alkynes with aryl or vinyl...
The Sonogashira reaction is a cross-coupling reaction of a vinyl or aryl halide with a terminal alky...
A novel supported catalyst formed by an oxime-derived palladacycle supported on clay OxPdCy@clay is ...
An MCM-48 supported 2-pyridinylmethanimine Pd-catalyst was found to be a highly efficient catalyst i...
The Pd–Cu catalysed Sonogashira coupling of terminal alkynes and aryl halides is a cornerstone synth...