Gualandi, Andrea’s team published research in Organic Chemistry Frontiers in 2018 | 3336-49-0

Organic Chemistry Frontiers published new progress about Aryl bromides Role: RCT (Reactant), RACT (Reactant or Reagent). 3336-49-0 belongs to class isoquinoline, and the molecular formula is C9H7NO, Quality Control of 3336-49-0.

Gualandi, Andrea; Savoini, Andrea; Saporetti, Roberto; Franchi, Paola; Lucarini, Marco; Cozzi, Pier Giorgio published the artcile< A facile hydroxylation of arylboronic acids mediated by sodium ascorbate>, Quality Control of 3336-49-0, the main research area is arylboronic acid sodium ascorbate hydroxylation green chem; phenol preparation.

A simple, direct and facile hydroxylation of arylboronic acids was described. The reaction was carried out under air, in an open flask, using 2 equiv of sodium ascorbate. A variety of arylboronic acids were transformed into the corresponding phenols in excellent to moderate isolated yields. The reaction tolerated the presence of functional groups, and mols. that are readily oxidized by H2O2 can be present in the reaction mixture This green methodol. avoids the use of photoredox conditions, transition metals, or other strong oxidants.

Organic Chemistry Frontiers published new progress about Aryl bromides Role: RCT (Reactant), RACT (Reactant or Reagent). 3336-49-0 belongs to class isoquinoline, and the molecular formula is C9H7NO, Quality Control of 3336-49-0.

Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem