Active anionic zero-valent palladium catalysts: characterization by density functional calculations.
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Transmetallation versus β-hydride elimination: the role of 1,4-benzoquinone in chelation-controlled arylation reactions with arylboronic acids.The Heck-Mizoroki cross-coupling reaction: a mechanistic perspective.Experiment and computation: a combined approach to study the reactivity of palladium complexes in oxidation states 0 to IV.The contribution of computational studies to organometallic catalysis: descriptors, mechanisms and models.Solvent effect on palladium-catalyzed cross-coupling reactions and implications on the active catalytic species.Anionic Palladium(0) and Palladium(II) Ate Complexes.Developing Synthetic Approaches with Non-Innocent Metalloligands: Easy Access to IrI/Pd0 and IrI/Pd0/IrI CoresPhosphine-free Heck reaction: mechanistic insights and catalysis “on water” using a charge-tagged palladium complexWhat makes for a good catalytic cycle? A theoretical study of the SPhos ligand in the Suzuki–Miyaura reaction
P2860
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P2860
Active anionic zero-valent palladium catalysts: characterization by density functional calculations.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
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2004年学术文章
@zh-hans
2004年学术文章
@zh-my
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name
Active anionic zero-valent pal ...... nsity functional calculations.
@en
Active anionic zero-valent pal ...... nsity functional calculations.
@nl
type
label
Active anionic zero-valent pal ...... nsity functional calculations.
@en
Active anionic zero-valent pal ...... nsity functional calculations.
@nl
prefLabel
Active anionic zero-valent pal ...... nsity functional calculations.
@en
Active anionic zero-valent pal ...... nsity functional calculations.
@nl
P50
P356
P1476
Active anionic zero-valent pal ...... nsity functional calculations.
@en
P2093
Sason Shaik
P304
P356
10.1002/CHEM.200306056
P407
P577
2004-06-01T00:00:00Z