906562-63-8

Upstream product

• 5396-89-4 benzyl acetoacetate 
• 10323-20-3 D-Arabinose 
• 58-86-6 D-xylose 
• 906562-62-7 benzyl 5-(3-O-tert-butyldiphenylsilyl-D-threo-1,2,3-trihydroxyprop-1-yl)-2-methylfuran-3-carboxylate 

Downstream Products

• 906562-65-0 benzyl 5-(1-azido-1-deoxy-D-erythro-1,2,3-trihydroxyprop-1-yl)-2-methylfuran-3-carboxylate 
• 906562-66-1 benzyl 5-[(R)-1-azido-2-hydroxyethyl]-2-methylfuran-3-carboxylate 
• 906562-64-9 benzyl 5-(1-azido-3-O-tert-butyldiphenylsilyl-1-deoxy-D-erythro-1,2,3-trihydroxyprop-1-yl)-2-methylfuran-3-carboxylate 
• 1235552-20-1 benzyl 5-(1-azido-3-O-tert-butyldiphenylsilyl-1-deoxy-D-threo-1,2,3-trihydroxyprop-1-yl)-2-methylfuran-3-carboxylate 

Relevant academic research and scientific papers

Stereoselective synthesis of chiral furan amino acid analogues of D- and L-serine from D-sugars

The synthesis of chiral furan amino acid analogues of D- and L-serine is reported. The developed methodology starting from D-xylose affords the corresponding amino acid derivative analogue of D-serine enantiomerically pure. Starting from D-arabinose, the

New methodology for the stereoselective synthesis of a-furfurylamines from sugars: Application to the synthesis of furyl amino acids and 3-Furylisoserines

The synthesis of two new furyl amino acids as rigid isosteres of the dipeptides (D)-H-Ser-(D, L)-Thr-OH and (L)-H-Ser-(D, L)Thr-OH is presented. The developed synthetic methodology starts from D-xylose and D-arabinose and makes use of trihydroxypropylfura