123100-66-3

Upstream product

• 98-01-1 furfural 
• 615-36-1 2-bromoaniline 

Downstream Products

• 123100-67-4 [(2-Allyl-[1,3]dithian-2-yl)-furan-2-yl-methyl]-(2-bromo-phenyl)-amine 
• 865353-82-8 (2-bromo-phenyl)-(1-furan-2-yl-but-3-enyl)-amine 
• 865353-70-4 (2-bromo-phenyl)-(1-furan-2-yl-3-methyl-but-3-enyl)-amine 
• 123100-68-5 C₁₈H₂₀BrNOS₂ 
• 123100-68-5 C₁₈H₂₀BrNOS₂ 

Relevant academic research and scientific papers

Novel approach to isoindolo[2,1-a]quinolines: Synthesis of 1- and 3-halo-substituted 11-oxo-5,6,6a,11-tetrahydroisoindolo[2,1-a]quinoline-10- carboxylic acids

A series of 1- and 3-halo-substituted isoindolo[2,1-a]quinolines were obtained by means of electrophilic cyclization of methallyl- and allyl-substituted isoindolo-7-carboxylic acids. The influence of halogen atoms on the stereochemistry of the formation o

Scope of Tandem Cycloaddition/Radical Cyclization Methodology

Tandem cycloaddition/radical cyclization is an effective strategy for the rapid assembly of a wide variety of ring systems.To set up the reagents for this sequence, it is necessary to include a potential radical site in one of the two cycloaddition partners, located at an appropriate distance from a new double bond that will be formed in the cycloaddition step.Examples in which the cycloaddition step is or and in which the radical cyclization creates 5-, 6-, or 7-membered rings are described.Examples of the tandem methodology carried out in a completely intramolecular mode are also described.