677300-91-3

Upstream product

• 100-52-7 benzaldehyde 
• 677300-65-1 (4R,5R,6R)-5-(tert-butyldimethylsilyloxy)-4-[(1S)-2-(tert-butyldimethylsilyloxy)-1-benzoyloxyethyl]-2,2-dimethyl-6-phenyl-[1,3]dioxane 
• 677300-58-2 (1S,3R,4R)-3-(tert-butyldimethylsilyloxy)-1-(tert-butyldimethylsilyloxymethyl)-4-hydroxy-2-oxo-4-phenylbutyl benzoate 
• 677300-63-9 (1S,2R,3R,4R)-3-(tert-butyldimethylsilyloxy)-1-(tert-butyldimethylsilyloxymethyl)-2,4-dihydroxy-4-phenylbutyl benzoate 
• 677300-71-9 (4R,5R,6R)-5-(tert-butyldimethylsilyloxy)-4-[(1S)-1,2-dihydroxyethyl]-2,2-dimethyl-6-phenyl-[1,3]dioxane 
• 677300-73-1 (4S,5R,6R)-5-(tert-butyldimethylsilyloxy)-2,2-dimethyl-6-phenyl-[1,3]dioxane-4-carbaldehyde 
• 677300-90-2 ethyl (E)-3-[(4R,5S,6R)-5-(tert-butyldimethylsilyloxy)-2,2-dimethyl-6-phenyl-[1,3]dioxan-4-yl]acrylate 
• 677300-67-3 (4R,5R,6R)-5-(tert-butyldimethylsilyloxy)-4-[(1S)-2-hydroxy-1-benzoyloxyethyl]-2,2-dimethyl-6-phenyl-[1,3]dioxane 

Relevant academic research and scientific papers

Stereoselective Anti Aldol Reactions of Erythrulose Derivatives. Functionalized Chiral d3 and d4 Synthons

An improved procedure for the synthesis of anti aldols from protected erythrulose derivatives is reported. The preparation of functionalized d 3 and d4 synthons with various stereochemical arrays by means of this methodology is descr