205489-15-2

Upstream product

• 100-39-0 benzyl bromide 
• 205489-14-1 (2S)-2-amino-2-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]ethan-1-ol 
• 205489-13-0 (R)-Azido-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-acetic acid ethyl ester 
• 205489-00-5 (R)-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-trifluoromethanesulfonyloxy-acetic acid ethyl ester 
• 114185-07-8 ethyl (2R)-2-[(1S)-3,3-dimethyl(2,4-dioxolanyl)]-2-hydroxyacetate 

Downstream Products

• 205489-17-4 (3S,4S)-4-Dibenzylamino-4-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-hydroxy-1-thiazol-2-yl-butan-1-one 
• 205489-16-3 (R)-Dibenzylamino-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-acetaldehyde 

Relevant academic research and scientific papers

Diastereoselective routes to side-chain truncated analogues of N-acetylneuraminic acid

Vitamin C 3 has been converted, in a completely stereo-controlled manner, into the side-chain truncated analogues 4 and 5 of N-acetylneuraminic acid 1.