501032-82-2

Upstream product

• 501032-71-9 (5S)-1-benzyl-5-phenyl-hexahydro-cyclopenta[c]isoxazole 
• 85027-81-2 (S)-3-phenylhex-5-enal 
• 184483-44-1 (4-Methoxy-phenyl)-((Z)-(S)-3-phenyl-hexa-1,5-dienyl)-carbamic acid tert-butyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 501032-81-1 (1S,2S,4S)-1-amino-N-benzyl-2-hydroxymethyl-4-phenylcyclopentane 

Downstream Products

• 1025927-97-2 (1R,2S,4S)-2-Benzylamino-4-phenyl-cyclopentanecarboxylic acid 
• 501032-84-4 (3S)-6-aza-6-benzyl-3-phenyl-bicyclo[3.2.0]heptan-7-one 
• 501032-83-3 (1R,2S,4S)-2-amino-N-benzyl-N-(tert-butoxycarbonyl)-4-phenyl-1-cyclopentanecarboxylic acid 

Relevant academic research and scientific papers

Synthetic applications of lithiated N-Boc allylic amines as asymmetric homoenolate equivalents

Lithiation of N-(Boc)-N-(p-methoxyphenyl) allylic amines in the presence of (-)-sparteine provides asymmetric homoenolate equivalents which react with electrophiles to provide highly enantioenriched enecarbamates. Acidic hydrolysis of the enecarbamates can provide the corresponding β-substituted aldehydes. A synthetic sequence that involves a stereocontrolled intramolecular nitrone-olefin dipolar cycloaddition has been developed for the preparation of enantioenriched 2-formyl-4-phenyl-1-aminocyclopentanes from one β-allyl-substituted aldehyde. Further manipulations allow access to an enantioenriched β-lactam. In another synthetic sequence, transmetalation of the lithiated intermediates and reactions with aldehyde electrophiles can be controlled to afford highly enantioenriched anti homoaldol products. Use of an anti aldehyde homoaldol product as the chiral electrophile in an iterative reaction provides a double homoaldol product containing four stereogenic centers with high diastereoselectivity and enantioselectivity. Reaction pathways are proposed to account for the observed products.