403666-52-4

Upstream product

• 403666-51-3 (1'S,1R,2S,5S)-2-(1'-phenylethoxy)-3-triethylsilanyloxy-8-oxabicyclo[3.2.1]octa-3,6-diene 
• 209852-87-9 (-)-(1'S,2S)-2α-(1-Phenylethoxy)-8-oxabicyclo[3.2.1]oct-6-en-3-one 

Downstream Products

• 403666-62-6 (1'S,1R,2S,3R,4R,5S)-(2-(1'-phenylethoxy)-3-(tert-butyldimethylsilanyloxy)-8-oxabicyclo[3.2.1]oct-6-en-4-yl) pivaloate 
• 403666-31-9 (1'S,1R,2R,3S,4S,5S)-(3-hydroxy-2-(1'-phenylethoxy)-8-oxabicyclo[3.2.1]oct-6-en-4-yl) pivaloate 
• 403666-32-0 (1'S,1R,2R,3R,4S,5S)-(3-hydroxy-2-(1'-phenylethoxy)-8-oxabicyclo[3.2.1]oct-6-en-4-yl) pivaloate 
• 403666-30-8 (1'S,1R,2S,4R,5S)-(2-(1'-phenylethoxy)-8-oxabicyclo[3.2.1]octa-6-ene-3-one-4-yl) pivaloate 
• 403666-53-5 (1'S,1R,2S,4S,5S)-(2-(1'-phenylethoxy)-8-oxabicyclo[3.2.1]oct-6-en-3-one-4-yl) pivaloate 

Relevant academic research and scientific papers

The Total Synthesis of C-Glycosides with Completely Resolved Seven-Carbon Backbone Polyol Stereochemistry: Stereochemical Correlations and Access to L-Configured and Other Rare Carbohydrates

The de novo synthesis of a full set of hydroxymethyl C-glycosides from only two precursors is described. The seven-carbon target molecules contain five stereocentres and bridge the stereochemical gap between natural D-configured and non-natural L-configur