1133798-41-0

Usage

Uses

Used in Organic Synthesis:
2,4,6-Tris(3,4-dichlorophenyl)boroxin is used as a reagent in organic synthesis for the preparation of functionalized molecules. Its unique structure allows for the creation of a variety of complex organic compounds, making it a valuable tool in the field of chemistry.
Used in Pharmaceutical Development:
2,4,6-Tris(3,4-dichlorophenyl)boroxin is used as a potential candidate in the development of new drugs and pharmaceuticals. Its chemical properties and reactivity make it a promising starting point for the synthesis of novel therapeutic agents.
Used in Research and Development:
2,4,6-Tris(3,4-dichlorophenyl)boroxin is used in research and development settings to explore its potential applications and properties. Its unique structure and reactivity provide opportunities for the discovery of new chemical reactions and the synthesis of innovative compounds.

Upstream product

• 151169-75-4 3,4-dichlophenylboronic acid 

Downstream Products

• 1133798-33-0 methyl 2-(3,4-dichlorophenyl)-2-p-tolylacetate 
• 1354729-12-6 C₂₃H₂₀Cl₂O 
• 1380035-68-6 C₂₂H₂₀Cl₂O₃S 
• 55039-68-4 4-(3,4-dichlorophenyl)morpholine 
• 80576-51-8 N,N-dibenzyl-3,4-dichloroaniline 
• 1358750-87-4 9-[4-(3,4-dichlorophenoxy)phenyl]-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide 

Relevant academic research and scientific papers

Scalable synthesis of oxazolones from propargylic alcohols through multistep palladium(II) catalysis: β-selective oxidative heck coupling of cyclic sulfonyl enamides and aryl boroxines

A whale of a scale: The title oxidative Heck coupling proceeded with unusual β selectivity to generate a variety of branched substituted oxazolones (see scheme; Ts=p-toluenesulfonyl). The three-step synthesis from readily available starting materials with a simple palladium catalyst and inexpensive reagents could be carried out in a single reaction vessel or scaled up for the preparation of large amounts of these amino acid precursors. Copyright

Transition-metal-free electrophilic amination of arylboroxines

A transition-metal-free strategy to construct C(sp2)-N bonds using arylboroxines and O-benzoyl hydroxylamines as coupling partners has been developed. This transformation provides a useful method to access various aromatic amines.

Arylation and vinylation of α-diazocarbonyl compounds with boroxines

An alternative approach for α-arylation and α-vinylation of carbonyl compounds is described: reaction between aryl-or vinylboroxines with α-diazocarbonyl compounds leads to the formation of α-arylated or α-vinylated carbonyl compounds under mild conditions.