Abstract Recent development of the palladium-catalyzed Stille cross-coupling reactions is reviewed, which includes (1) the reactions of organotin compounds with organic electrophilic reagents such as aro-matic halides, alkyl halides, and acyl chlorides etc., (2) mechanisms of the palladium-catalyzed Stille reac-tion, and (3) the applications of the Stille reaction to organic synthesis
Solvent-free protocols for palladium-catalyzed stannylation of aryl halides, Stille cross-coupling, ...
The Stille cross-coupling of allylic and benzyl bromides is shown to proceed efficiently using phosp...
Cross-coupling reactions, such as the Stille reaction of organostannanes [1–3] and the Suzuki (or Su...
Stille reaction is one of the most common, efficient and selective Pd-catalyzed cross-coupling react...
Producción CientíficaThe first now named Stille reaction was published 38 years ago, and the last c...
Organic chemistry is present in all domains of everyday life, from polymer production to medicine. I...
The palladium-catalyzed Stille coupling reaction was used for preparing functionalized, conjugated p...
A water-soluble PdCl2(NH3)2/cationic 2,2′-bipyridyl system was found to be a highly efficient cataly...
An inexpensive and new triphenylphosphine-based palladacycle has been developed as a pre-catalyst le...
The present thesis deals with various types of palladium(II) and platinum(II) complexes and their us...
1380-1387A Pd-based heterogeneous catalyst (Pd(II)-MCM-41) derived from post-synthesis modification...
In an improved procedure, the complex {2,6-bis[(diphenylphosphino)methyl]benzene}chloropalladium(II)...
The relative reactivities of vinylstannanes 2a,b and 4a,b in a Stille coupling with vinyl bromide we...
Aryl sulfamates, tosylates, and mesylates undergo efficient Ni-catalyzed cross coupling with diverse...
An inexpensive and new triphenylphosphine‐based palladacycle has been developed as a pre‐catalyst le...
Solvent-free protocols for palladium-catalyzed stannylation of aryl halides, Stille cross-coupling, ...
The Stille cross-coupling of allylic and benzyl bromides is shown to proceed efficiently using phosp...
Cross-coupling reactions, such as the Stille reaction of organostannanes [1–3] and the Suzuki (or Su...
Stille reaction is one of the most common, efficient and selective Pd-catalyzed cross-coupling react...
Producción CientíficaThe first now named Stille reaction was published 38 years ago, and the last c...
Organic chemistry is present in all domains of everyday life, from polymer production to medicine. I...
The palladium-catalyzed Stille coupling reaction was used for preparing functionalized, conjugated p...
A water-soluble PdCl2(NH3)2/cationic 2,2′-bipyridyl system was found to be a highly efficient cataly...
An inexpensive and new triphenylphosphine-based palladacycle has been developed as a pre-catalyst le...
The present thesis deals with various types of palladium(II) and platinum(II) complexes and their us...
1380-1387A Pd-based heterogeneous catalyst (Pd(II)-MCM-41) derived from post-synthesis modification...
In an improved procedure, the complex {2,6-bis[(diphenylphosphino)methyl]benzene}chloropalladium(II)...
The relative reactivities of vinylstannanes 2a,b and 4a,b in a Stille coupling with vinyl bromide we...
Aryl sulfamates, tosylates, and mesylates undergo efficient Ni-catalyzed cross coupling with diverse...
An inexpensive and new triphenylphosphine‐based palladacycle has been developed as a pre‐catalyst le...
Solvent-free protocols for palladium-catalyzed stannylation of aryl halides, Stille cross-coupling, ...
The Stille cross-coupling of allylic and benzyl bromides is shown to proceed efficiently using phosp...
Cross-coupling reactions, such as the Stille reaction of organostannanes [1–3] and the Suzuki (or Su...