868756-22-3

Upstream product

• 868756-10-9 N,N-diethyl 2-formyl-4,6-dimethoxybenzamide 
• 868756-20-1 7-(benzyloxy)-1-bromoundec-10-ene 
• 91-52-1 2,4 dimethoxybenzoic acid 
• 142601-55-6 N,N-diethyl-2,4-dimethoxybenzamide 
• 39828-35-8 2,4-dimethoxybenzoyl chloride 
• 868756-18-7 7-(benzyloxy)-1-(tert-butyldimethylsilyloxy)undec-10-ene 
• 868756-11-0 N,N-diethyl 4,6-dimethoxy-2-(1'-hydroxypent-4'-en-1'-yl)benzamide 
• 868756-17-6 1-(tert-butyldimethylsilyloxy)undec-10-en-7-ol 
• 868756-19-8 7-(benzyloxy)undec-10-en-1-ol 
• 868756-12-1 3-(but-3'-en-1'-yl)-5,7-dimethoxy-(3H)-isobenzofuran-1-one 
• 868756-16-5 tert-butyl-dimethyl-(6-oxiranyl-hexyloxy)-silane 
• 868756-03-0 5,7-dimethoxy-3-(3'-oxoprop-1'-yl)-(3H)-isobenzofuran-1-one 
• 868756-15-4 tert-butyl dimethyl(oct-7-en-1-yloxy)silane 
• 868756-21-2 3-(10'-benzyloxytetradec-3',13'-dien-1'-yl)-5,7-dimethoxy-(3H)-isobenzofuran-1-one 

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