52814-52-5

Upstream product

• 75226-99-2 [5-methoxy-2-(4-methoxy-benzoyl)-phenoxy]-acetic acid 
• 5298-27-1 (2,4-dihydroxyphenyl)(4-methoxyphenyl)methanone 
• 52814-89-8 α-(3-methoxyphenoxy)-4-methoxyacetophenone 
• 150-19-6 O-methylresorcine 
• 52688-74-1 potassium 3-methoxyphenolate 
• 108-46-3 recorcinol 
• 100-07-2 4-methoxy-benzoyl chloride 
• 6131-38-0 2-hydroxy-4,4'-dimethoxybenzophenone 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 

Downstream Products

• 60312-34-7 6-methoxy-3-(4-methoxy-phenyl)-benzofuran-2-carbaldehyde 
• 74229-12-2 4-((6-methoxy-3-(4-methoxyphenyl)benzofuran-2-yl) methyl)morpholine 
• 35983-60-9 6-methoxy-3-(4-methoxy-phenyl)-benzofuran-2-carboxylic acid 
• 120990-51-4 [6-hydroxy-3-(4-hydroxyphenyl)-1-benzofuran-2-yl](4-hydroxyphenyl)methanone 
• 120990-50-3 <6-methoxy-3-(4-methoxyphenyl)-1-benzofuran-2-yl>(4-methoxyphenyl)methanone 

Relevant academic research and scientific papers

Facile synthesis of 3-aryl benzofurans, 3-aryl benzothiophenes, 2-aryl indoles and their dimers

The preparation of 3-aryl benzofuran and benzothiophenes and their dimers at 2-position and, 2-aryl indoles and their 3-position dimers preparation is described.

Ga(OTf)3-mediated synthesis of substituted benzofurans

A synthetic procedure, for the synthesis of a series of functionalized benzofurans 3–5 and benzonaphthofurans 6, starting from intermolecular O-alkylation of α-bromoaryl ketones 2 with potassium oxygenated phenoxides 1 followed by Ga(OTf)3-catalyzed direct intramolecular cyclodehydration of the resulting α-aryloxyaryl ketones, has been developed. The use of various metal triflates was investigated for a facile approach and efficient transformation. Pentacyclic benzophenanthrofurans 7 were prepared via photolytic annulations of 5.

Structure-activity relationship of antiestrogens: A study using triarylbutenone, benzofuran, and triarylfuran analogues as models for triarylethylenes and triarylpropenones

In a study of the structure-activity relationship (SAR) of antiestrogens use has been made of certain 1,2,3-triarylbutenones, of 2-arylbenzofurans carrying aryl or aroyl substituents at C3, and of 2,3,4-triarylfurans as conformationally constra