877438-72-7

Upstream product

• 877438-62-5 (3R)-3-[(propane-1,3-diyldithio)-(4-tert-butyldimethylsilanyloxy-4-methoxyphenyl)methyl]butano-4-lactone 
• 97315-20-3 3-<(tert-butyldimethylsilyl)oxy>-4-methoxybenzyl bromide 
• 97315-18-9 p-methoxy-m-(tert-butyldimethylsilyloxy)-benzaldehyde 
• 877438-55-6 (3R,4R)-3-[(propane-1,3-diyldithio)-(3-tert-butyldimethylsilanyloxy-4-methoxyphenyl)methyl]-4-[(1R,2S,5R)-2-(1-methylethyl)-5-methyl-1-cyclohexyloxy]butano-4-lactone 
• 877438-48-7 2-(3-tert-butyldimethylsilanyloxy-4-methoxyphenyl)-1,3-dithiane 

Downstream Products

• 877438-80-7 (8R,8'R)-3,3'-bis(tert-butyldimethylsilanyloxy)-4,4'-dimethoxy-7'-oxolignano-9,9'-lactone 

Relevant academic research and scientific papers

Asymmetric synthesis, stereochemistry and rearrangement reactions of naturally occurring 7′-hydroxylignano-9,9′-lactones

The asymmetric synthesis of a series of (7′S,8R,8′R)-7′- hydroxylignano-9,9′-lactones is presented, among them the mammalian lignan (7′S)-hydroxyenterolactone and (7′S)-parabenzlactone, allowing the stereochemistry of natural occurring (-)-parabenzlactone