847550-67-8

Upstream product

• 34143-74-3 1H,1H,2H,2H-Perfluorodecanethiol 
• 847550-77-0 5-bromo-3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecane-1-sulfonyl)-1-propyl-1,3-dihydroindol-2-one 
• 847550-40-7 5-bromo-3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecane-1-sulfonyl)-1-propyl-1,3-dihydroindole-2-one 
• 929540-89-6 N-(4-bromo-phenyl)-2-oxo-N-propyl-acetamide 
• 847550-62-3 5-bromo-3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecylsulfonyl)-3-methyl-1-propyl-1,3-dihydroindol-2-one 
• 5720-05-8 4-methylphenylboronic acid 

Relevant academic research and scientific papers

A fluorous, pummerer cyclative-capture strategy for the synthesis of N-heterocycles

A fluorous, cyclative-capture strategy based on a new Pummerer cyclization process allows rapid access to tagged, heterocyclic frameworks. Convenient modification of the fluorous, heterocyclic scaffolds by using a variety of approaches including Pd-catalyzed cross-couplings is possible. Traceless, reductive cleavage of the fluorous-phase tag or oxidative cleavage and further elaboration, completes a strategy for the high-throughput, fluorous-phase synthesis of a diverse range of N-heterocycles.

A fluorous-phase Pummerer cyclative-capture strategy for the synthesis of nitrogen heterocycles

Catching on: Fluorous-tagged heterocyclic frameworks accessed rapidly through a Pummerer cyclative-capture approach can then be modified conveniently, for example, by Pd-catalyzed cross-coupling. Traceless, reductive cleavage of the fluorous phase tag com