868756-18-7

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 13175-44-5 oct-7-en-1-ol 
• 868756-16-5 tert-butyl-dimethyl-(6-oxiranyl-hexyloxy)-silane 
• 868756-15-4 tert-butyl dimethyl(oct-7-en-1-yloxy)silane 
• 868756-17-6 1-(tert-butyldimethylsilyloxy)undec-10-en-7-ol 
• 100-39-0 benzyl bromide 

Downstream Products

• 868756-22-3 3-(10'-benzyloxy-13'-oxotetradec-3'-en-1'-yl)-5,7-dimethoxy-(3H)-isobenzofuran-1-one 
• 868756-21-2 3-(10'-benzyloxytetradec-3',13'-dien-1'-yl)-5,7-dimethoxy-(3H)-isobenzofuran-1-one 
• 868756-20-1 7-(benzyloxy)-1-bromoundec-10-ene 
• 868756-19-8 7-(benzyloxy)undec-10-en-1-ol 

Relevant academic research and scientific papers

Synthesis of the phthalide-containing anti-Helicobacter pylori agents CJ-13,015, CJ-13,102, CJ-13,103, CJ-13,104 and CJ-13,108

Flexible racemic syntheses of the phthalide-containing antibiotics CJ-13,015, CJ-13,102, CJ-13,103, CJ-13,104 and CJ-13,108 that inhibit Helicobacter pylori have been carried out in a convergent fashion by Wittig coupling of a phthalide-containing aldehyd