1452153-47-7

Upstream product

• 637-69-4 4-Methoxystyrene 
• 5813-57-0 2-acetyl-1,4-naphthoquinone 
• 105379-29-1 methyl 1-hydroxy-4-methoxy-2-naphthoate 
• 77060-74-3 methyl 1,4-dihydroxy-2-naphthoate 
• 31519-22-9 1,4-dihydroxy-2-naphthoic acid 
• 83575-14-8 2-methoxycarbonyl-1,4-naphthoquinone 

Relevant academic research and scientific papers

Antioxidant and antibacterial evaluation of synthetic furomollugin and its diverse analogs

Diverse furomollugin (3) and its analogs (11-22) were synthesized in high yields via ceric ammonium nitrate-catalyzed formal [3 + 2] cycloaddition as a key step. The in vitro antioxidant activities of synthesized compounds were determined by analyzing rad

Dihydronaphtho[1,2-b]furan derivatives and synthesis method thereof

The present invention relates to dihydronaphtho[1,2-b]furan derivatives and a synthesis method thereof, wherein different kinds of dihydronaphtho[1,2-b]furan derivatives representing various biological activities can be synthesized through a one-pot process with high yield. In addition, the synthesized dihydronaphtho[1,2-b]furan can be easily synthesized using a key step to furumollugin in a second step.COPYRIGHT KIPO 2015

USE OF SUBSTITUTED 2,3-DIHYDRO-1-BENZOFURAN-4-CARBOXYLIC ACIDS OR SALTS THEREOF AS ACTIVE SUBSTANCES AGAINST ABIOTIC PLANT STRESS

Use of substituted 2,3-dihydro-1-benzofuran-4-carboxylic acids of the general formula (I) or salts thereof where the radicals in the general formula (I) are as defined in the description, for increasing stress tolerance in plants with respect to abiotic

A novel and efficient synthesis of diverse dihydronaphtho[1,2-b]furans using the ceric ammonium nitrate-catalyzed formal [3 + 2] cycloaddition of 1,4-naphthoquinones to olefins and its application to furomollugin

A novel approach was developed for the synthesis of diverse dihydronaphtho[1,2-b]furans from 1,4-naphthoquinones and olefins in the presence of ceric ammonium nitrate. This reaction provides a rapid route for the synthesis of a variety of dihydronaphtho[1,2-b]furans and naphtho[1,2-b]furans bearing different substituents. This methodology was also used to synthesize the biologically important natural product furomollugin in only 2 steps. The Royal Society of Chemistry.