A single phosphine ligand allows palladium-catalyzed intermolecular C-O bond formation with secondary and primary alcohols.
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Mild and general palladium-catalyzed synthesis of methyl aryl ethers enabled by the use of a palladacycle precatalystA new biarylphosphine ligand for the Pd-catalyzed synthesis of diaryl ethers under mild conditions.Design of New Ligands for the Palladium-Catalyzed Arylation of α-Branched Secondary Amines.Combined oxypalladation/C-H functionalization: palladium(II)-catalyzed intramolecular oxidative oxyarylation of hydroxyalkenes.Evidence for in situ catalyst modification during the Pd-catalyzed conversion of aryl triflates to aryl fluorides.Investigating the dearomative rearrangement of biaryl phosphine-ligated Pd(II) complexes.An Improved Synthesis of BrettPhos and RockPhos-Type Biarylphosphine Ligands.Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands.Room temperature, metal-free arylation of aliphatic alcohols.Oxidative coupling of sp 2 and sp 3 carbon-hydrogen bonds to construct dihydrobenzofurans.Alkyl Aryl Ether Bond Formation with PhenoFluor.Oxidative Addition Complexes as Precatalysts for Cross-Coupling Reactions Requiring Extremely Bulky Biarylphosphine Ligands.Nickel-Catalyzed Intramolecular C-O Bond Formation: Synthesis of Cyclic Enol Ethers.Late-Stage Diversification of Biologically Active Molecules via Chemoenzymatic C-H Functionalization.Synthesis of Ethers via Reaction of Carbanions and Monoperoxyacetals.Oxidative addition to palladium(0) diphosphine complexes: observations of mechanistic complexity with iodobenzene as reactant.Copper-catalyzed dehydrogenative coupling of arenes with alcohols.Palladium-Catalyzed Fluorination of Cyclic Vinyl Triflates: Effect of TESCF3 as an Additive.Site-Selective O-Arylation of Glycosides.Palladium-Catalyzed 2,2,2-Trifluoroethoxylation of Aromatic and Heteroaromatic Chlorides Utilizing Borate Salt and the Synthesis of a Trifluoro Analogue of Sildenafil.Synthesis of Complex Phenols Enabled by a Rationally Designed Hydroxide Surrogate.Palladium-Catalyzed C-O Cross-Coupling of Primary Alcohols.Cobalt-catalyzed C(sp(2))-H alkoxylation of aromatic and olefinic carboxamides.Palladium-Catalyzed Methoxylation of Aromatic Chlorides with Borate SaltsPalladium(0)-Catalyzed Intermolecular Arylative Dearomatization of β-Naphthols.BippyPhos: a single ligand with unprecedented scope in the Buchwald-Hartwig amination of (hetero)aryl chlorides.Synthesis and Characterization of a Bidirectional Photoswitchable Antagonist Toolbox for Real-Time GPCR Photopharmacology.
P2860
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P2860
A single phosphine ligand allows palladium-catalyzed intermolecular C-O bond formation with secondary and primary alcohols.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh
2011年學術文章
@zh-hant
name
A single phosphine ligand allo ...... econdary and primary alcohols.
@ast
A single phosphine ligand allo ...... econdary and primary alcohols.
@en
type
label
A single phosphine ligand allo ...... econdary and primary alcohols.
@ast
A single phosphine ligand allo ...... econdary and primary alcohols.
@en
prefLabel
A single phosphine ligand allo ...... econdary and primary alcohols.
@ast
A single phosphine ligand allo ...... econdary and primary alcohols.
@en
P2093
P2860
P356
P1476
A single phosphine ligand allo ...... econdary and primary alcohols.
@en
P2093
Brett P Fors
Stephen L Buchwald
Xiaoxing Wu
P2860
P304
P356
10.1002/ANIE.201104361
P407
P577
2011-09-12T00:00:00Z