342646-88-2

Upstream product

• 54974-07-1 phthalimidesulfenyl chloride 
• 197248-10-5 di-tertiary-butyldimethylsilane phloroglucinol 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 342646-97-3 5,7-bis-(tert-butyl-dimethyl-silanyloxy)-2,3-dihydro-2-(4-methoxy-phenyl)-1,4-benzoxathiin 
• 848933-32-4 5,7-bis-(tert-butyl-dimethyl-silanyloxy)-2-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2,3-dihydro-benzo[1,4]oxathiine 
• 848933-37-9 5,7-bis-(tert-butyl-dimethyl-silanyloxy)-2,3-dihydro-2-(4-methoxy-phenyl)-1,4-benzoxathiin 4,4-dioxide 
• 865541-49-7 5,7-bis-(tert-butyl-dimethyl-silanyloxy)-2-[3,4-bis-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2,3-dihydro-1,4-benzoxathiin 

Relevant academic research and scientific papers

Synthesis and "double-faced" antioxidant activity of polyhydroxylated 4-thiaflavans

A simple synthetic methodology, based on the inverse electron demand hetero Diels-Alder reaction of electron-poor dienic o-thioquinones with electron-rich styrenes used as dienophiles, allowed the preparation of several polyhydroxylated 4-thiaflavans. Suc

Easy synthesis of polyphenolic 4-thiaflavans with a 'double-faced' antioxidant activity

Inverse electron demanding Diels-Alder reactions of o-thioquinones with styrenes, followed by simple manipulations of the obtained cycloadducts, allowed the synthesis of polyphenolic 4-thiaflavans which showed antioxidant activity miming either flavonoid