Wu, Shaofeng; Geng, Furong; Dong, Jianyu; Liu, Long; Su, Lebin; Zhou, Yongbo published the artcile< General and practical synthesis of naphtho[2,1-d]oxazoles from naphthols and amines>, Product Details of C7H8BrN, the main research area is naphthol amine oxidative cyclization; naphthooxazole preparation.
A general and practical synthesis of naphtho[2,1-d]oxazoles from readily available naphthols and amines was developed using TEMPO as the oxygen source with outstanding functional group tolerance, especially for the construction of the naphthoxazole-related bioactive mol. PBNI and naphthoxazole-doped materials, as well as the polyaryloxazole-related ADN derivative This protocol allowed the rapid assembly of a small library of naphtho[2,1-d]oxazole skeletons (55 examples) that are difficult to be prepared by other methods. The ESR (EPR) and 18O-labeled experiments indicated that the radical adducts of TEMPO with naphthalenone radicals may serve as key intermediates.
Organic Chemistry Frontiers published new progress about Aromatic alcohols Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 3959-07-7 belongs to class bromides-buliding-blocks, and the molecular formula is C7H8BrN, Product Details of C7H8BrN.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary