70874-62-3

Upstream product

• 89-84-9 2',4'-dihydroxy-4-acetophenone 
• 4697-62-5 6-bromohomoveratric acid 
• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 
• 91377-14-9 4-(3'-hydroxy-4'-methoxyphenyl)-6-formyl-7-hydroxy-5-methoxy-2H-1-benzopyran-2-one, voludal 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 76322-30-0 ethyl(4,5-dimethoxy-2-hydroxyphenyl)acetate 
• 5252-40-4 3-hydroxy-8,9-dimethoxycoumestan 
• 76322-22-0 ethyl(2-ethoxycarbonylmethoxy-4,5-methoxyphenyl)acetate 
• 328314-29-0 4-benzyloxycarbonyl-6,7-dimethoxy-4-(2,4,6-trimethoxyphenyl)-2H-1-benzopyran-3(4H)-one 
• 328314-28-9 4-benzyloxycarbonyl-6,7-dimethoxy-4-(2,4-dimethoxyphenyl)-2H-1-benzopyran-3(4H)-one 
• 328314-27-8 4-benzyloxycarbonyl-6,7-dimethoxy-4-(4-methoxyphenyl)-2H-1-benzopyran-3(4H)-one 
• 328314-32-5 6,7-dimethoxy-4-(2,4,6-trimethoxyphenyl)-2H-1-benzopyran-3(4H)-one 
• 328314-20-1 4-benzyloxycarbonyl-6,7-dimethoxy-2H-1-benzopyran-3(4H)-one 
• 97341-39-4 methyl (2-methoxycarbonylmethoxy-4,5-dimethoxyphenyl)acetate 

Relevant academic research and scientific papers

Copper-catalyzed intramolecular cross dehydrogenative coupling approach to coumestans from 2′-hydroxyl-3-arylcoumarins

A copper-catalyzed intramolecular cross dehydrogenative C-O coupling reaction of 2′-hydroxyl-3-arylcoumarins was developed. This protocol provided a facile and efficient strategy for the construction of natural coumestans and derivatives in moderate to high yields. This transformation exhibited good functional group compatibility and was amenable to substrates with free phenolic hydroxyl groups.

New Phenolic Components from Dalbergia Volubilis

Phytochemical examination of non green branches of Dalbergia volubilis on extensive column and preparative thin layer chromatography yielded twelve compounds eight of which are already known compounds and were identified as sitosterol, 7-hydroxy-4-methyl-coumarin, dalbergin, biochanin-A, umbelliferone, p-hydroxy cinnamic acid, kaempferol and quercetin-3-O-glucoside.The other four compounds were new natural products, three of which were identified as novel 4-phenyl-2H-1-benzopyran-2-ones while the fourth one was a new 12a-hydroxy rotenoid.The structure of these new compounds has been established on the basis of chemical and spectral evidences and through derivatization, as 4',7-dihydroxy-3'-methoxy-4-phenyl-2H-1-benzopyran-2-one, 3',7-dihydroxy-4',5-dimethoxy-2H-1-benzopyran-2-one, 3',7-dihydroxy4',5-dimethoxy-6-formyl-2H-1-benzopyran-2-one and a complex rotenoid determined to be as (VII).The co-occurence of 4-methyl-2H-1-benzopyran-2-ones, 4-phenyl-2H-1-benzopyran-2-ones, isoflavones and rotenoids is of interest from biogenetic considerations.