757241-92-2

Upstream product

• 45157-84-4 S-t-butyl-L-cysteine t-butyl ester 
• 1694-92-4 2-Nitrobenzenesulfonyl chloride 

Downstream Products

• 1151800-70-2 N-(2,3,5-tri-O-acetyl-α-L-arabinofuranos-1-yl)-N-(2-nitrobenzenesulfonyl)-S-t-butyl-L-cysteine t-butyl ester 
• 1151800-73-5 N-(2,3,5-tri-O-acetyl-β-L-arabinofuranos-1-yl)-N-(2-nitrobenzenesulfonyl)-S-t-butyl-L-cysteine t-butyl ester 

Relevant academic research and scientific papers

Stereoselective synthesis of novel N-(α-l-arabinofuranos-1-yl)-l-amino acids

In lead detoxification, the α-anomer of N-glycocyl-l-amino acid is more potent than its β-anomer. Here a six-step-reaction route for stereoselectively preparing N-(α-l-arabinose-1-yl)-l-amino acids is reported. Treating l-arabinose with acetic anhydride a