332386-76-2

Upstream product

• 1486-47-1 3,4,5-tris(benzyloxy)benzoyl chloride 
• 332386-73-9 (+)-(2S,3S)-cis-5,7-bis(benzyloxy)-2-[3,4,5-tris(benzyloxy)phenyl]chroman-3-ol 
• 332386-57-9 (1R,2R)-3-[2,4-Bis-benzyloxy-6-(tert-butyl-dimethyl-silanyloxy)-phenyl]-1-(3,4,5-tris-benzyloxy-phenyl)-propane-1,2-diol 
• 332386-70-6 (+)-(2S,3R)-trans-5,7-bis(benzyloxy)-2-[3,4,5-tris(benzyloxy)phenyl]chroman-3-ol 
• 332386-61-5 (E)-3-[2,4-bis(benzyloxy)-6-hydroxyphenyl]-1-[3,4,5-tris(benzyloxy)phenyl]-propene 
• 332386-78-4 (S)-5,7-Bis-benzyloxy-2-(3,4,5-tris-benzyloxy-phenyl)-chroman-3-one 
• 332386-68-2 (E)-3-[3,4,5-tris(benzyloxy)phenyl]prop-2-en-1-ol 
• 70424-94-1 methyl 3,4,5-tris(benzyloxy)benzoate 
• 1486-48-2 3,4,5-tribenzyloxybenzoic acid 
• 79831-88-2 3,4,5-tribenzyloxybenzyl alcohol 
• 332386-67-1 ethyl (E)-3,4,5-tris(benzyloxy)cinnamate 
• 332386-55-7 (E)-3-[2,4-bis(benzyloxy)-6-(tert-butyldimethylsilyloxy)phenyl]-1-[3,4,5-tris(benzyloxy)phenyl]propene 
• 1027171-15-8 3,5-Bis-benzyloxy-2-[(4R,5R)-2-ethoxy-5-(3,4,5-tris-benzyloxy-phenyl)-[1,3]dioxolan-4-ylmethyl]-phenol 
• 332386-59-1 (+)-(1R,2R)-3-[2,4-bis(benzyloxy)-6-hydroxyphenyl]-1-[3,4,5-tris(benzyloxy)phenyl]propane-1,2-diol 

Relevant academic research and scientific papers

Enantioselective synthesis of epigallocatechin-3-gallate (EGCG), the active polyphenol component from green tea.

[reaction: see text]. Enantioselective synthesis of epigallocatechin-3-gallate (EGCG, 3b), the active polyphenol component from green tea, has been achieved by using a stereospecific cyclization of the Sharpless asymmetric dihydroxylation product 7c as the key step.