1785-66-6

Upstream product

• 93-59-4 Perbenzoic acid 
• 90-15-3 α-naphthol 
• 135-19-3 β-naphthol 
• 83-72-7 2-hydroxynaphtho-1,4-quinone 
• 98-88-4 benzoyl chloride 
• 95525-97-6 2,2-bis(benzoyloxy)-1(2H)-naphthalenone 

Relevant academic research and scientific papers

Synthesis, biological evaluation, and correlation of cytotoxicity versus redox potential of 1,4-naphthoquinone derivatives

A series of 1,4-naphthoquinone derivatives of lawsone (1), 6-hydroxy-1,4-naphthoquinone (2), and juglone (3) were synthesized by alkylation, acylation, and sulfonylation reactions. The yields of lawsone derivatives 1a-1k (type A), 6-hydroxy-1,4-naphthoqui

Highly Active Manganese-Mediated Acylation of Alcohols with Acid Chlorides or Anhydrides

To explore further the practical uses of highly active manganese (Mn?), a variety of alcohols were treated with Mn?, and the resulting complexes were coupled with acid chlorides and/or acetic anhydride in the absence of any extra catalyst. The subsequent reactions took place smoothly under mild conditions, providing the corresponding O-acylation products in good to excellent isolated yields.

The Oxidation of Some Naphthols with Benzoyl Peroxide

The reactions of four naphthols (1-naphthol (1), 2-naphthol (2), 4-isopropyl-1-naphthol (18), and 3-isopropyl-2-naphthol (19)) with benzoyl peroxide were examined under two reaction conditions (A and B).Each of the naphthols 1,2,18, and 19 was oxidized wi