Hajra, Saumen published the artcileBronsted Acid Promoted Regioselective C-3 Arylation and Heteroarylation of Spiro-epoxyoxindoles for the Construction of All Carbon Quaternary Centres: A Detailed Study, Product Details of C8H10O2, the main research area is spiroepoxyoxindole heteroarene carbon quaternary center trifluoroacetic acid Friedel Crafts; oxindole derivative regioselective green preparation.
An efficient strategy for the synthesis of all carbon quaternary centers has been developed via Bronsted acid-promoted highly regioselective intermol. Friedel-Crafts reactions of heteroarenes or arenes with spiro-epoxyoxindoles. In addition, we have successfully performed the ring opening reaction in relatively cheap condition using water as a solvent. Beneficially, we have utilized the methodol. as the key step for the synthesis of advanced precursors of various natural and unnatural indole alkaloids.
European Journal of Organic Chemistry published new progress about Aromatic hydrocarbons Role: RCT (Reactant), RACT (Reactant or Reagent). 151-10-0 belongs to class isoquinoline, name is 1,3-Dimethoxybenzene, and the molecular formula is C8H10O2, Product Details of C8H10O2.
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem