| scholarly article | Q13442814 |
| P50 | author | Stephen L. Buchwald | Q6134174 |
| P2093 | author name string | Brett P Fors | |
| Xiaoxing Wu | |||
| P2860 | cites work | Efficient palladium-catalyzed coupling reactions of aryl bromides and chlorides with phenols | Q82299245 |
| A general and efficient catalyst for palladium-catalyzed C-O coupling reactions of aryl halides with primary alcohols | Q84621347 | ||
| Formation of ArF from LPdAr(F): catalytic conversion of aryl triflates to aryl fluorides | Q24626698 | ||
| An Efficient Intermolecular Palladium-Catalyzed Synthesis of Aryl Ethers | Q29039095 | ||
| Palladium-Catalyzed C−O Coupling Involving Unactivated Aryl Halides. Sterically Induced Reductive Elimination To Form the C−O Bond in Diaryl Ethers | Q30053746 | ||
| Pd-catalyzed N-arylation of secondary acyclic amides: catalyst development, scope, and computational study | Q33586499 | ||
| Pd-catalyzed cross-coupling reactions of amides and aryl mesylates | Q33870854 | ||
| Pd-catalyzed O-arylation of ethyl acetohydroximate: synthesis of O-arylhydroxylamines and substituted benzofurans | Q34065855 | ||
| Palladium-Catalyzed Conversion of Aryl and Vinyl Triflates to Bromides and Chlorides | Q34287143 | ||
| Pd-catalyzed amidation of aryl chlorides using monodentate biaryl phosphine ligands: a kinetic, computational, and synthetic investigation. | Q34698998 | ||
| Pd-catalyzed conversion of aryl chlorides, triflates, and nonaflates to nitroaromatics | Q35001565 | ||
| A highly active catalyst for Pd-catalyzed amination reactions: cross-coupling reactions using aryl mesylates and the highly selective monoarylation of primary amines using aryl chlorides | Q37356701 | ||
| Palladium-catalyzed formation of aryl tert-butyl ethers from unactivated aryl halides | Q43561884 | ||
| Palladium-catalyzed intramolecular C-O bond formation | Q43816123 | ||
| Copper(I)-catalyzed aryl bromides to form intermolecular and intramolecular carbon-oxygen bonds. | Q45992849 | ||
| General, mild, and intermolecular Ullmann-type synthesis of diaryl and alkyl aryl ethers catalyzed by diol-copper(I) complex | Q46053937 | ||
| An improved Cu-based catalyst system for the reactions of alcohols with aryl halides | Q46877393 | ||
| Significantly improved method for the pd-catalyzed coupling of phenols with aryl halides: understanding ligand effects | Q48694094 | ||
| Copper-catalyzed coupling of aryl iodides with aliphatic alcohols | Q50191933 | ||
| N- versus O-arylation of aminoalcohols: orthogonal selectivity in copper-based catalysts | Q79885447 | ||
| Use of tunable ligands allows for intermolecular Pd-catalyzed C--O bond formation | Q81801097 | ||
| P433 | issue | 42 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | palladium | Q1089 |
| P304 | page(s) | 9943-9947 | |
| P577 | publication date | 2011-09-12 | |
| P1433 | published in | Angewandte Chemie International Edition | Q62023953 |
| P1476 | title | A single phosphine ligand allows palladium-catalyzed intermolecular C-O bond formation with secondary and primary alcohols | |
| P478 | volume | 50 |
| Q35691917 | A new biarylphosphine ligand for the Pd-catalyzed synthesis of diaryl ethers under mild conditions |
| Q41529179 | Alkyl Aryl Ether Bond Formation with PhenoFluor |
| Q36713972 | An Improved Synthesis of BrettPhos and RockPhos-Type Biarylphosphine Ligands |
| Q54528959 | BippyPhos: a single ligand with unprecedented scope in the Buchwald-Hartwig amination of (hetero)aryl chlorides. |
| Q53392746 | Cobalt-catalyzed C(sp(2))-H alkoxylation of aromatic and olefinic carboxamides. |
| Q35945017 | Combined oxypalladation/C-H functionalization: palladium(II)-catalyzed intramolecular oxidative oxyarylation of hydroxyalkenes |
| Q45206680 | Copper-catalyzed dehydrogenative coupling of arenes with alcohols |
| Q35812271 | Design of New Ligands for the Palladium-Catalyzed Arylation of α-Branched Secondary Amines |
| Q35967391 | Evidence for in situ catalyst modification during the Pd-catalyzed conversion of aryl triflates to aryl fluorides |
| Q36489784 | Investigating the dearomative rearrangement of biaryl phosphine-ligated Pd(II) complexes. |
| Q41966650 | Late-Stage Diversification of Biologically Active Molecules via Chemoenzymatic C-H Functionalization |
| Q34359682 | Mild and general palladium-catalyzed synthesis of methyl aryl ethers enabled by the use of a palladacycle precatalyst |
| Q41861362 | Nickel-Catalyzed Intramolecular C-O Bond Formation: Synthesis of Cyclic Enol Ethers. |
| Q41588880 | Oxidative Addition Complexes as Precatalysts for Cross-Coupling Reactions Requiring Extremely Bulky Biarylphosphine Ligands. |
| Q43497416 | Oxidative addition to palladium(0) diphosphine complexes: observations of mechanistic complexity with iodobenzene as reactant |
| Q41353559 | Oxidative coupling of sp 2 and sp 3 carbon-hydrogen bonds to construct dihydrobenzofurans. |
| Q54103017 | Palladium(0)-Catalyzed Intermolecular Arylative Dearomatization of β-Naphthols. |
| Q48103371 | Palladium-Catalyzed 2,2,2-Trifluoroethoxylation of Aromatic and Heteroaromatic Chlorides Utilizing Borate Salt and the Synthesis of a Trifluoro Analogue of Sildenafil. |
| Q52688495 | Palladium-Catalyzed C-O Cross-Coupling of Primary Alcohols. |
| Q46495211 | Palladium-Catalyzed Fluorination of Cyclic Vinyl Triflates: Effect of TESCF3 as an Additive |
| Q53999982 | Palladium-Catalyzed Methoxylation of Aromatic Chlorides with Borate Salts |
| Q38974125 | Room temperature, metal-free arylation of aliphatic alcohols |
| Q47362050 | Site-Selective O-Arylation of Glycosides. |
| Q55232052 | Synthesis and Characterization of a Bidirectional Photoswitchable Antagonist Toolbox for Real-Time GPCR Photopharmacology. |
| Q37030381 | Synthesis and application of palladium precatalysts that accommodate extremely bulky di-tert-butylphosphino biaryl ligands |
| Q48366114 | Synthesis of Complex Phenols Enabled by a Rationally Designed Hydroxide Surrogate. |
| Q43119887 | Synthesis of Ethers via Reaction of Carbanions and Monoperoxyacetals |
| Q87388350 | Synthesis of an electron-rich KITPHOS monophosphine, preparation of derived metal complexes and applications in catalysis |
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