1062148-82-6

Basic information

• Product Name: 3,4-diisobutyl 2-methyl (2S,3S,4S,5R)-5-phenylpyrrolidine-2,3,4-tricarboxylate
• Synonyms: 3,4-diisobutyl 2-methyl (2S,3S,4S,5R)-5-phenylpyrrolidine-2,3,4-tricarboxylate
• CAS NO: 1062148-82-6
• Molecular Weight: 405.491
• Mol File: 1062148-82-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3,4-diisobutyl 2-methyl (2S,3S,4S,5R)-5-phenylpyrrolidine-2,3,4-tricarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-diisobutyl 2-methyl (2S,3S,4S,5R)-5-phenylpyrrolidine-2,3,4-tricarboxylate(1062148-82-6)
• EPA Substance Registry System: 3,4-diisobutyl 2-methyl (2S,3S,4S,5R)-5-phenylpyrrolidine-2,3,4-tricarboxylate(1062148-82-6)

Safety Data

• Hazardous Substances Data: 1062148-82-6(Hazardous Substances Data)

Upstream product

• 7283-69-4 di-isobutylfumarate 
• 14234-82-3 diisobutyl maleate 
• 66646-88-6 methyl 2-(benzylideneamino)acetate 

Relevant articles and documents

Synthesis of prolines by enantioselective 1,3-dipolar cycloaddition of azomethine ylides and alkenes catalyzed by chiral phosphoramidite-silver(I) complexes

The endo-diastereo- and enantioselective 1,3-dipolar cyclo-addition of azomethine ylides and electrophilic alkenes is ef-ficiently catalysed by chiral phosphoramidite-silver(I) Per-chlorate complexes. The reaction allows the presence of dif-ferent types o

Catalytic enantioselective 1,3-dipolar cycloaddition reactions of azomethine ylides and alkenes by using phosphoramidite-silver(I) complexes

(Chemical Presented) Silver catalysts: A novel chiral phosphoramidite -silver perchlorate complex has been used for the synthesis of highly substituted pyrolidine rings. This method is valuable for the synthesis of biologically active α-substituted prolines by using hindered dipoles generated from α-substituted α amino acids (see scheme; DABCO=1,4-diazabicyclo[2.2.2]octane).