66417-41-2

Upstream product

• 6626-15-9 4-Bromoresorcinol 
• 75-36-5 acetyl chloride 
• 108-05-4 vinyl acetate 
• 108-24-7 acetic anhydride 

Downstream Products

• 66417-51-4 (E)-3-(2,4-Diacetoxy-phenyl)-acrylic acid methyl ester 
• 673477-44-6 6-(2'-(2'',4''-diacetoxyphenyl)ethynyl)-1-methoxy-3,4-methylenedioxybenzene 
• 504422-00-8 acetic acid 5-acetoxy-2-phenylethynyl-phenyl ester 
• 673477-40-2 1,3-diacetoxy-4-trimethylsilylethynylbenzene 
• 134937-20-5 2-(3,5-dimethoxyphenyl)-6-hydroxybenzofuran 
• 56317-21-6 moracin M 
• 135248-05-4 5-[6-hydroxy-5-(3-methylbut-2-en-1-yl)-1-benzofuran-2-yl]benzene-1,3-diol 

Relevant academic research and scientific papers

Effective synthetic method of natural product moracin N

The present invention relates to a method of efficiently synthesizing moracin N which is a small amount in mulberry tree leaves and has an antibacterial activity, including development of a method of efficiently synthesizing moracin N by developing a meth

Facile synthesis of natural moracin compounds using PD(OAC)2/P(TBU)3-HBF4 as a sonogashira coupling reagent

An efficient and practical synthesis of natural moracins, which have diverse range of biological properties including anticancer, antioxidant, and antibacterial activities, has been achieved using Pd(OAc)2/P(tBu)3-HBF

The first total synthesis of Cicerfuran utilizing a one-pot synthesis of hydroxylated benzofurans

A simple one-pot procedure was elaborated for the preparation of hydroxylated benzofurans from halogenated phenols and was successfully applied to the first total synthesis of Cicerfuran, a natural defence agent of wild chickpea.

Lipase-catalyzed regioselective protection of hydroxyl groups in aromatic dihydroxyaldehydes and ketones

Pseudomonas cepacia lipase catalyzes the acetylation in organic solvent of dihydroxyaldehydes and ketones using vinyl acetate as acyl donor. The method is completely regioselective and allows to obtain partially acetylated compounds different from those obtained by enzymic hydrolysis of polyacetoxy arylaldehydes and ketones.