Pages that link to "Q34287143"

The following pages link to Palladium-Catalyzed Conversion of Aryl and Vinyl Triflates to Bromides and Chlorides (Q34287143):

Displaying 26 items.

• Reductive functionalization of a rhodium(III)-methyl bond by electronic modification of the supporting ligand (Q30457819) (← links)
• An improved palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides (Q35206680) (← links)
• Evidence for in situ catalyst modification during the Pd-catalyzed conversion of aryl triflates to aryl fluorides (Q35967391) (← links)
• A unified route to the welwitindolinone alkaloids: total syntheses of (-)-N-methylwelwitindolinone C isothiocyanate, (-)-N-methylwelwitindolinone C isonitrile, and (-)-3-hydroxy-N-methylwelwitindolinone C isothiocyanate (Q36011847) (← links)
• Lessons Learned while Traversing the Welwitindolinone Alkaloids Obstacle Course (Q36212300) (← links)
• A single phosphine ligand allows palladium-catalyzed intermolecular C-O bond formation with secondary and primary alcohols (Q36300984) (← links)
• Investigating the dearomative rearrangement of biaryl phosphine-ligated Pd(II) complexes. (Q36489784) (← links)
• An Improved Synthesis of BrettPhos and RockPhos-Type Biarylphosphine Ligands (Q36713972) (← links)
• Studies toward welwitindolinones: formal syntheses of N-methylwelwitindolinone C isothiocyanate and related natural products (Q37109025) (← links)
• Addressing challenges in palladium-catalyzed cross-coupling reactions through ligand design (Q38025590) (← links)
• Mechanistic insights on the Pd-catalyzed addition of C-X bonds across alkynes - a combined experimental and computational study (Q38815698) (← links)
• Iron(III)-mediated photocatalytic selective substitution of aryl bromine by chlorine with high chloride utilization efficiency. (Q39267319) (← links)
• Computational Study of the Palladium-Catalyzed Carbonylative Synthesis of Aromatic Acid Chlorides: The Synergistic Effect of PtBu3 and CO on Reductive Elimination (Q39409824) (← links)
• Pd-Catalyzed Decarbonylative Cross-Couplings of Aroyl Chlorides (Q41475265) (← links)
• Facile conversion of chromane-6-triflate to chromane-6-alanines under Palladium conditions (Q43240941) (← links)
• Harnessing reversible oxidative addition: application of diiodinated aromatic compounds in the carboiodination process (Q45341114) (← links)
• Synthesis and Applications of Cyclohexenyl Halides Obtained by a Cationic Carbocyclisation Reaction. (Q48160704) (← links)
• C-H carbonylation: In situ acyl triflates ace it. (Q49849388) (← links)
• A DFT Study on the Conversion of Aryl Iodides to Alkyl Iodides: Reductive Elimination of R-I from Alkylpalladium Iodide Complexes with Accessible β-Hydrogens. (Q51547601) (← links)
• Nucleophile promoted gold redox catalysis with diazonium salts: C–Br, C–S and C–P bond formation through catalytic Sandmeyer coupling† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c6sc01742h. (Q55717003) (← links)
• Chemoselectivity in the Kosugi-Migita-Stille coupling of bromophenyl triflates and bromo-nitrophenyl triflates with (ethenyl)tributyltin (Q57825512) (← links)
• The role of organometallic copper(iii) complexes in homogeneous catalysis (Q59287892) (← links)
• Total Synthesis of (-)-Nodulisporic Acids D, C, and B: Evolution of a Unified Synthetic Strategy (Q59508665) (← links)
• Visible-Light-Induced Palladium-Catalyzed Generation of Aryl Radicals from Aryl Triflates (Q90187399) (← links)
• A copper-mediated reverse aromatic Finkelstein reaction in ionic liquid (Q90478719) (← links)
• Metathesis-active ligands enable a catalytic functional group metathesis between aroyl chlorides and aryl iodides (Q90788671) (← links)