2006
DOI: 10.1002/adsc.200690004
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Cover Picture: On the Nature of the Active Species in Palladium Catalyzed Mizoroki–Heck and Suzuki–Miyaura Couplings – Homogeneous or Heterogeneous Catalysis, A Critical Review: (Adv. Synth. Catal. 6/2006)

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Cited by 16 publications
(28 citation statements)
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“…The Heck reaction is a palladium catalyzed cross-coupling of aromatic halides with alkenes as shown in Scheme 2 [23,24] and it has been considered as the most powerful and versatile method for the construction of the sp 2 esp 2 carbonecarbon bonds for the synthesis of stereoselective alkenes with various interesting pharmacological, biological, or physical properties [25]. Although the Heck reaction tolerates a wide variety of functional groups on both reactants, it generally requires ligands such as phosphines to stabilize the palladium-based catalytic center to prevent the formation of the palladium black since palladium aggregation will dramatically decrease the catalytic activities.…”
Section: Pd/pcms Catalyzed Heck Cross-coupling Of Aromatic Halides Wimentioning
confidence: 99%
“…The Heck reaction is a palladium catalyzed cross-coupling of aromatic halides with alkenes as shown in Scheme 2 [23,24] and it has been considered as the most powerful and versatile method for the construction of the sp 2 esp 2 carbonecarbon bonds for the synthesis of stereoselective alkenes with various interesting pharmacological, biological, or physical properties [25]. Although the Heck reaction tolerates a wide variety of functional groups on both reactants, it generally requires ligands such as phosphines to stabilize the palladium-based catalytic center to prevent the formation of the palladium black since palladium aggregation will dramatically decrease the catalytic activities.…”
Section: Pd/pcms Catalyzed Heck Cross-coupling Of Aromatic Halides Wimentioning
confidence: 99%
“…Since the Heck type reaction was first published almost 40 years ago [4,5], several thousand articles referring to it have been published. Many of these articles deal with the development of new palladium catalysts (both homogeneous and heterogeneous) [6][7][8][9], reaction conditions such as solvents, bases, and additives, mechanistic and kinetic studies, and the use of microwave irradiation as the heat source [10][11][12][13]. However, to our knowledge, no one has investigated how ultraviolet (UV) and/or visible (vis) irradiation influences the Heck reaction.…”
Section: Introductionmentioning
confidence: 98%
“…Since ligand-free Pd turned out to be feasible for the Heck reaction on aryl iodides [5], extensive studies of ligandfree Pd catalyzed Heck reactions on aryl halides have increasingly been appearing [2,[6][7][8][9][10]. Due to the drawbacks with homogeneous catalysts, it has been desirable to develop heterogeneous Heck reaction catalysts for industrial applications and notable progress has been seen in this area [6,9,10]. Instead of organic ligands, ligand-free catalyst systems use inexpensive bases such as NaOAc, Na 2 CO 3 , NaHCO 3 , Ca(OH) 2 , K 3 PO 3 , and amines, etc.…”
Section: Introductionmentioning
confidence: 99%