57020-97-0

Upstream product

• 603-76-9 1-methylindole 
• 3558-24-5 1-methyl-2-phenyl-1H-indole 
• 611-10-9 2-ethoxycarbonyl-1-cyclopentanone 
• 98-80-6 phenylboronic acid 
• 621-23-8 1,2,3-trimethoxybenzene 

Downstream Products

• 3128-05-0 (3-oxo-cyclopentyl)-acetic acid 
• 2630-44-6 3-(hydroxycarbonylmethyl)cyclopentan-1-one 
• 2630-37-7 3-(hydroxycarbonylmethyl)cyclopentan-1-one 
• 68882-71-3 2-(hydroxymethyl)cyclopent-2-enone 
• 66655-93-4 (+/-)-dehydropentenomycin 
• 68907-79-9 (+/-)-Pentenomycin I 
• 68907-80-2 (+/-)-pentenomycin II 
• 77480-52-5 (+/-)-epipentenomycin I 
• 80963-19-5 α-(hydroxymethyl)cyclopentenone ethylene ketal 
• 76047-51-3 (5-oxocyclopent-1-en-1-yl)methyl acetate 
• 4581-74-2 neonepetalactone 
• 4581-74-2 neonepetalactone 
• 3558-24-5 1-methyl-2-phenyl-1H-indole 
• 1425314-03-9 (5S)-ethyl 2-oxo-5-((R)-5-oxo-2,5-dihydrofuran-2-yl)cyclopentanecarboxylate 

Relevant academic research and scientific papers

A three-component palladium-catalyzed oxidative C-C coupling reaction: A domino process in two dimensions

Easy as ABC. or CBA! Indoles can be selectively functionalized twice by a catalytic oxidative three-component coupling of arylboronates and β-ketoesters. The difference in the rates (see scheme) of the competing processes are amplified under the conditions of the three-component reaction. Copyright

Palladium-catalyzed dehydrogenative β′-arylation of β-keto esters under aerobic conditions: Interplay of metal and Bronsted acids

The Bronsted aids: The first dehydrogenative arylation of β-keto esters with arenes under ambient aerobic conditions is described (see scheme). Under a PdII/Bronsted acid co-catalytic system, regioselective arylations with alkoxylated arenes an