1443278-02-1

Basic information

• Product Name: ethyl (1S,3R,3aS,6aR)-4,6-dioxo-3-(p-methoxyphenyl)-5-phenyloctahydropyrrole[3,4-c]pyrrole-1-carboxylate
• Synonyms: ethyl (1S,3R,3aS,6aR)-4,6-dioxo-3-(p-methoxyphenyl)-5-phenyloctahydropyrrole[3,4-c]pyrrole-1-carboxylate
• CAS NO: 1443278-02-1
• Molecular Weight: 394.427
• Mol File: 1443278-02-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl (1S,3R,3aS,6aR)-4,6-dioxo-3-(p-methoxyphenyl)-5-phenyloctahydropyrrole[3,4-c]pyrrole-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (1S,3R,3aS,6aR)-4,6-dioxo-3-(p-methoxyphenyl)-5-phenyloctahydropyrrole[3,4-c]pyrrole-1-carboxylate(1443278-02-1)
• EPA Substance Registry System: ethyl (1S,3R,3aS,6aR)-4,6-dioxo-3-(p-methoxyphenyl)-5-phenyloctahydropyrrole[3,4-c]pyrrole-1-carboxylate(1443278-02-1)

Safety Data

• Hazardous Substances Data: 1443278-02-1(Hazardous Substances Data)

Upstream product

• 941-69-5 N-phenyl-maleimide 
• 52141-94-3 [(4-methoxybenzylidene)-amino]-acetic acid ethyl ester 

Relevant articles and documents

Synthesis of new chiral ferrocenyl P,N-ligands with a benzoxazole ring and their application in Ag-catalyzed asymmetric [3+2] cycloaddition

New chiral ferrocenyl P,N-ligands with a benzoxazole ring as the N-donor group have been synthesized from 2-aminophenol through a three-step transformation and successfully employed in the Ag-catalyzed asymmetric [3+2] cycloaddition of azomethine ylides with electron-deficient alkenes. High diastereoselectivities, excellent enantioselectivities, and good yields have been achieved for a variety of substrates, demonstrating the potential of these new P,N-ligands in asymmetric catalysis.