915779-91-8

Upstream product

• 222420-87-3 (+/-)-methyl 4-formyl-2,3-dihydro-1H-pyrrole-2-carboxylate 
• 24424-99-5 di-tert-butyl dicarbonate 
• 915779-85-0 4-(tert-butyldimethylsilanyloxymethyl)-2,3-dihydropyrrole-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester 
• 915779-99-6 4-hydroxymethyl-2,3-dihydropyrrole-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester 
• 915779-84-9 4-formyl-2,3-dihydropyrrole-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester 
• 915779-86-1 4-(tert-butyldimethylsilanyloxymethyl)-2,3-dihydropyrrole-1,2-dicarboxylic acid 1-tert-butyl ester 

Downstream Products

• 915779-96-3 2-[(4-benzoyloxymethyl-1-tert-butoxycarbonyl-2,3-dihydro-1H-pyrrole-2-carbonyl)(benzyl)amino]-malonic acid diethyl ester 
• 915779-93-0 2-[benzyl-(1-tert-butoxycarbonyl-4-hydroxymethyl-2,3-dihydro-1H-pyrrole-2-carbonyl)amino]-malonic acid diethyl ester 
• 915779-92-9 2-{benzyl[1-tert-butoxycarbonyl-4-(tert-butyldimethylsilanyloxymethyl)-2,3-dihydro-1H-pyrrole-2-carbonyl]amino}malonic acid diethyl ester 

Relevant academic research and scientific papers

π-Allyl palladium approach toward the diazabicyclo[3.2.1]octane core of the naphthyridinomycin alkaloids

A novel and efficient protocol for the synthesis of the 3,8-diazabicyclo[3.2.1]octane system found in the naphthyridinomycin, dnacin, and tetrazomine families of alkaloids is described. The key transformation involves an intramolecular palladium-catalyzed