115915-06-5

Upstream product

• 100-39-0 benzyl bromide 
• 103795-10-4 (2R,3R)-1,2-O-Isopropylidene-3-(2-thiazolyl)-1,2,3-propanetriol 
• 15186-48-8 2,3-isopropylidene-glyceraldehyde 
• 118377-11-0 2-[(S)-Benzyloxy-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-methyl]-3-methyl-thiazol-3-ium; iodide 
• 142760-44-9 2-[(1S,2S)-1,2-Bis-benzyloxy-2-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethyl]-thiazole 
• 142705-77-9 (2S,3R)-2-benzyloxy-3,4-isopropylidenedioxy-1-(2-thiazolyl)-1-butanone 
• 142760-41-6 (1R,2R)-2-Benzyloxy-2-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-thiazol-2-yl-ethanol 
• 142705-75-7 2-[(S)-Benzyloxy-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-methyl]-thiazole 
• 104470-54-4 (1S,2R)-2,3-O-isopropylidene-1-(2-thiazolyl)-1,2,3-propanetriol 
• 118319-71-4 ((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-thiazol-2-yl-methanone 
• 108275-55-4 (S)-Benzyloxy-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-acetaldehyde 

Relevant academic research and scientific papers

Construction of all O-alkoxy D-tetrose and D-pentose stereoisomers from 2,3-O-isopropylidene-D-glyceraldehyde using 2-(trimethylsilyl)thiazole as a formyl anion equivalent

All D-tetroses and D-pentoses having differentially protected hydroxy groups are synthesized by an iterative one-carbon chain-elongation cycle commencing with the addition of 2-(trimethylsilyl)thiazole to 2,3-O-isopropylidene-D-glyceraldehyde. One half of