1344660-00-9

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 140-88-5 ethyl acrylate 
• 3132-99-8 m-bromobenzoic aldehyde 

Downstream Products

• 1344660-28-1 (S,E)-ethyl 2-(3-bromobenzylidene)-4-nitropentanoate 
• 1381859-98-8 (S)-tert-butyl 1-[(S)-1-(3-bromophenyl)-2-(ethoxycarbonyl)allyl]-3-oxo-1,3-dihydroisobenzofuran-1-carboxylate 
• 1395055-46-5 C₂₈H₂₀BrNO₆ 
• 1386412-97-0 (3aR,4S,6aS)-ethyl 4-(3-bromophenyl)-1,3-dioxo-2-phenyl-1,2,3,3a,4,6a-hexahydrocyclopenta[c]pyrrole-5-carboxylate 

Relevant academic research and scientific papers

Direct Synthesis of Dihydropyrrolo[2,1-a]Isoquinolines through FeCl3 Promoted Oxidative Aromatization

We have developed a straightforward FeCl3 promoted synthesis of dihydropyrrolo[2,1-a]isoquinolines through formal (3+2) cycloaddition/oxidative aromatization cascade of dihydroisoquinoline with Morita-Baylis-Hillman carbonates (up to 96% yield)

Catalytic Enantioselective Vinylogous Allylic Alkylation of Coumarins

An unprecedented, organocatalytic enantioselective vinylogous γ-allylic alkylation of 4-methylcoumarins has been developed. Using allylic carbonates as the allyl source, this reaction is catalyzed by Lewis basic dimeric Cinchona alkaloid (QD)2P