Stille coupling involving bulky groups feasible with gold cocatalyst.
about
Polymer [Pd(CH2SO2C6H4Me)2]n, a precursor to remarkably stable Pd organometallics.Synthesis and characterization of fluorinated azadipyrromethene complexes as acceptors for organic photovoltaics.Experiment and computation: a combined approach to study the reactivity of palladium complexes in oxidation states 0 to IV.Rationale for the sluggish oxidative addition of aryl halides to Au(I).Au(i)/Ag(i) co-operative catalysis: interception of Ag-bound carbocations with α-gold(i) enals in the imino-alkyne cyclizations with N-allenamides.Role of Lewis acid additives in a palladium catalyzed directed C-H functionalization reaction of benzohydroxamic acid to isoxazolone.The decisive role of ligand metathesis in Au/Pd bimetallic catalysis.Merging gold catalysis, organocatalytic oxidation, and Lewis acid catalysis for chemodivergent synthesis of functionalized oxazoles from N-propargylamides.In Situ Generation of ArCu from CuF2 Makes Coupling of Bulky Aryl Silanes Feasible and Highly Efficient.Gold catalyzed Heck-coupling of arenediazonium o-benzenedisulfonimides.Dramatic mechanistic switch in Sn/Au(I) group exchanges: transmetalation vs. oxidative addition.An unexpected transmetalation intermediate: isolation and structural characterization of a solely CH3 bridged di-copper(i) complex.Direct evidence for intermolecular oxidative addition of σ(Si-Si) bonds to gold.A theoretical DFT-based and experimental study of the transmetalation step in Au/Pd-mediated cross-coupling reactions.
P2860
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
P2860
Stille coupling involving bulky groups feasible with gold cocatalyst.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Stille coupling involving bulky groups feasible with gold cocatalyst.
@en
Stille coupling involving bulky groups feasible with gold cocatalyst.
@nl
type
label
Stille coupling involving bulky groups feasible with gold cocatalyst.
@en
Stille coupling involving bulky groups feasible with gold cocatalyst.
@nl
prefLabel
Stille coupling involving bulky groups feasible with gold cocatalyst.
@en
Stille coupling involving bulky groups feasible with gold cocatalyst.
@nl
P2093
P2860
P50
P356
P1476
Stille coupling involving bulky groups feasible with gold cocatalyst.
@en
P2093
Desirée Carrasco
Juan delPozo
Mónica H Pérez-Temprano
Rosana Álvarez
P2860
P304
P356
10.1002/ANIE.201209262
P407
P577
2013-01-22T00:00:00Z