Bag, Sukdev published the artcilePalladium-Catalyzed Selective meta-C-H Deuteration of Arenes: Reaction Design and Applications, Product Details of C9H10O3, the main research area is phenylacetic acid deuteriated acetic palladium catalyst regioselective deuteration; deuteriated phenylacetic acid preparation; benzylsulfonic acid deuteriated acetic palladium catalyst regioselective deuteration; benzyl sulfonic acid deuteriated preparation; C−H activation; deuterium; pharmaceuticals; pyrimidine-based directing group; template synthesis.
An easily removable pyrimidine-based auxiliary was employed for the meta-C-H deuteration of arenes. The scope of this Pd-catalyzed deuteration using com. available [D1]- and [D4]-acetic acid was demonstrated by its application in phenylacetic acid and phenylmethanesulfonate derivatives A detailed mechanistic study led to explore the reversibility of the non-rate determining C-H activation step. The of meta-deuterium incorporation illustrated the template morphol. in terms of selectivity. The applicability of this method was demonstrated by the selective deuterium incorporation into various pharmaceuticals.
Chemistry – A European Journal published new progress about Carboxylic esters Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 104-01-8 belongs to class isoquinoline, name is 4-Methoxyphenylacetic acid, and the molecular formula is C9H10O3, Product Details of C9H10O3.
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem