1026575-47-2

Upstream product

• 844865-29-8 (1R,2R,3R,4S)-3-[Benzyl-(4-methoxy-benzyloxycarbonyl)-amino]-7-oxa-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid benzyl ester 
• 844865-51-6 (1R,2R,3R,4S)-3-Benzylamino-7-oxa-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid benzyl ester 
• 844865-30-1 (1R,2R,3R,4S)-3-(benzylamino)-7-oxa-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid 
• 104-88-1 4-chlorobenzaldehyde 
• 88333-03-3 Benzyl isocyanide 
• 844865-35-6 (1R,2R,3R,4S)-3-{Benzyl-[(S)-benzylcarbamoyl-(4-chloro-phenyl)-methyl]-amino}-7-oxa-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid methyl ester 

Downstream Products

• 844865-42-5 N-benzyl-2-benzylamino-2-(4-chloro-phenyl)-acetamide 

Relevant academic research and scientific papers

A novel highly selective chiral auxiliary for the asymmetric synthesis of L- and D-α-amino acid derivatives via a multicomponent ugi reaction

(Chemical Equation Presented) This paper describes the synthesis of a bicyclic β-amino acid scaffold in both pure enantiomeric forms and its application as chiral auxiliary in an intramolecular version of the Ugi multicomponent reaction (U-5C-4CR) to prepare α-amino acid derivatives of both D- and L-series in a straightforward and very stereoselective manner. The mild conditions required for the Ugi condensation and for the removal of the chiral auxiliary make this method very attractive to prepare a wide range of differently structured N-alkylated and unalkylated amino acid derivatives.