107658-27-5Relevant articles and documents
A soluble polymer-supported triflating reagent: a high-throughput synthetic approach to aryl and enol triflates.
Wentworth,Wentworth Jr.,Mansoor,Janda
, p. 477 - 480 (2000)
[reaction: see text] The high-yielding synthesis and application of the first example of a polymer-supported reagent for the preparation of trifluoromethanesulfonates (triflates) is described. This new reagent efficiently triflates aryl alcohols and lithi
Palladium Catalysed Alkoxycarbonylation of Phenols to Benzoate Esters
Dolle, Roland E.,Schmidt, Stanley J.,Kruse, Lawrence I.
, p. 904 - 905 (1987)
The methoxycarbonylation of aryl trifluoromethanesulphonates with CO and aliphatic alcohols is catalysed by Pd(OAc)2-1,3-bis(diphenylphosphino)propane in high yield at 70 deg C and ambient CO pressure.
Solvent-free ruthenium-catalysed triflate coupling as a convenient method for selective azole-o-C-H monoarylation
Abidi, Oumaima,Boubaker, Taoufik,Hierso, Jean-Cyrille,Roger, Julien
supporting information, p. 5916 - 5919 (2019/06/24)
Metal-catalysed ortho-directed C-H functionalization usually faces selectivity issues in the competition between mono- and disubstitution processes. We report herein the ruthenium-catalysed N-directed C-H monoarylation of arylpyrazoles with a selectivity
Pd-Catalyzed Conjunctive Cross-Coupling between Grignard-Derived Boron “Ate” Complexes and C(sp2) Halides or Triflates: NaOTf as a Grignard Activator and Halide Scavenger
Lovinger, Gabriel J.,Aparece, Mark D.,Morken, James P.
supporting information, p. 3153 - 3160 (2017/03/11)
Catalytic enantioselective conjunctive cross-couplings that employ Grignard reagents are shown to furnish an array of nonracemic chiral organoboronic esters in an efficient and highly selective fashion. The utility of sodium triflate in facilitating this reaction is two-fold: it enables “ate” complex formation and overcomes catalytic inhibition by halide ions.
