103795-35-3

Upstream product

• 103795-14-8 (1R)-2-O-benzyl-3,4-O-isopropylidene-1-(2-thiazolyl)-D-erythritol 
• 100-39-0 benzyl bromide 
• 103795-12-6 (R)-2-(benzyloxy)-2-[(R)-2,2-dimethyl-1,3-dioxolan-4-yl]acetaldehyde 
• 103795-11-5 (1R)-1-O-benzyl-2,3-O-isopropylidene-1-(2-thiazolyl)-D-glycitol 
• 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-[(R)-Benzyloxy-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-methyl]-3-methyl-thiazol-3-ium; iodide 
• 118377-12-1 2-[(R)-Benzyloxy-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-methyl]-3-methyl-thiazolidine 
• 103795-13-7 2-[(1R,2R)-2-Benzyloxy-2-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-trimethylsilanyloxy-ethyl]-thiazole 

Downstream Products

• 103795-36-4 (3S,4R)-3-O-benzyl-4,5-O-isopropylidene-3,4,5-trihydroxypentanal 
• 118377-26-7 2-O-benzyl-1-(2-thiazolyl)-2,3-butanediol 
• 118397-61-8 2,4,6-Trimethyl-benzenesulfonic acid (2R,3S)-3-benzyloxy-2-hydroxy-4-thiazol-2-yl-butyl ester 

Relevant academic research and scientific papers

Iterative, Stereoselective Homologation of Chiral Polyalkoxy Aldehydes Employing 2-(Trimethylsilyl)thiazole as a Formyl Anion Equivalent. The Thiazole Route to Higher Carbohydrates

A new approach to long-chain sugars is demonstrated by the stereoselective conversion of D-glyceraldehyde acetonide (2a), L-threose acetonide (2b), and dialdogalactopyranose diacetonide (2h) into higher homologues up to C9, C7, and C