162356-20-9

Basic information

• Product Name: (S)-2-(2-phenyl)ethenylpyrrolidine
• CAS NO: 162356-20-9
• Molecular Weight: 173.258
• Mol File: 162356-20-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (S)-2-(2-phenyl)ethenylpyrrolidine(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-(2-phenyl)ethenylpyrrolidine(162356-20-9)
• EPA Substance Registry System: (S)-2-(2-phenyl)ethenylpyrrolidine(162356-20-9)

Safety Data

• Hazardous Substances Data: 162356-20-9(Hazardous Substances Data)

Upstream product

• 198218-71-2 (S)-N-(tert-butoxycarbonyl)-2-(2-phenyl)ethenylpyrrolidine 
• 147-85-3 L-proline 
• 69610-41-9 Boc-L-Pro-H 
• 59936-29-7 (S)-N-(tert-butoxycarbonyl)proline methyl ester 
• 15761-39-4 1-(tert-butoxycarbonyl)-L-proline 
• 4706-43-8 1-benzyl-1H-benzotriazole 

Downstream Products

• 198218-79-0 1-[(S)-2-((E)-Styryl)-pyrrolidin-1-yl]-pent-4-en-1-one 

Relevant articles and documents

Synthesis of Chiral Bicyclic Lactams Using Ring Closure Metathesis: Synthesis of (-)-Coniceine and (S)-Pyrrolam A

Chiral (-)-coniceine and (S)-pyrrolam A were synthesized from dienes prepared from L-proline by ring closure metathesis.

Stereochemical consequences of the Lewis acid-promoted 3-aza-cope rearrangement of N-alkyl-N-allyl enamines

Internal and relative asymmetric induction were examined for the electrophile promoted 3-aza-Cope rearrangement of substituted N-alkyl-N-allyl enamines. In general, internal asymmetric induction was highly variable, and was dependent both upon the nature