88121-62-4

Basic information

• Product Name: (3aS,4S,9aR,9bR)-4-Benzoyl-2-phenyl-3a,4,9a,9b-tetrahydro-pyrrolo[3,4-a]indolizine-1,3-dione
• Synonyms: (3aS,4S,9aR,9bR)-4-Benzoyl-2-phenyl-3a,4,9a,9b-tetrahydro-pyrrolo[3,4-a]indolizine-1,3-dione
• CAS NO: 88121-62-4
• Molecular Weight: 370.408
• Mol File: 88121-62-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (3aS,4S,9aR,9bR)-4-Benzoyl-2-phenyl-3a,4,9a,9b-tetrahydro-pyrrolo[3,4-a]indolizine-1,3-dione(CAS DataBase Reference)
• NIST Chemistry Reference: (3aS,4S,9aR,9bR)-4-Benzoyl-2-phenyl-3a,4,9a,9b-tetrahydro-pyrrolo[3,4-a]indolizine-1,3-dione(88121-62-4)
• EPA Substance Registry System: (3aS,4S,9aR,9bR)-4-Benzoyl-2-phenyl-3a,4,9a,9b-tetrahydro-pyrrolo[3,4-a]indolizine-1,3-dione(88121-62-4)

Safety Data

• Hazardous Substances Data: 88121-62-4(Hazardous Substances Data)

Upstream product

• 941-69-5 N-phenyl-maleimide 
• 36377-40-9 pyridinium benzoylmethylide 
• 16883-69-5 N-phenacylpyridinium bromide 

Downstream Products

• 90625-60-8 3-(2-oxo-2-phenyl-ethylidene)-1-phenyl-pyrrolidine-2,5-dione 

Relevant articles and documents

Cycloaddition of Pyridinium Methylides with Electron-Deficient Olefins and Silica-Gel Mediated Elimination of Pyridines from the Cycloadducts: A New Method of Alkylation or Hydroalkylidenation of Olefins

Pyridinium methylides bearing an anion-stabilizing substituent at the ylide carbon react with a variety of olefins carrying two electron-withdrawing groups at the both carbons such as N-substituted maleimides, a citraconimide, dimethyl maleate, dimethyl f

STEREOSELECTIVE HYDROALKYLIDENATION OF OLEFIN WITH PYRIDINIUM METHYLIDES

Acid-catalyzed elimination of pyridine from the stereoselective cycloadducts between electron-deficient olefins and pyridinium methylides with ylide-stabilizing substituents offers a new type of C-C bond formation.