606926-18-5

Upstream product

• 444816-13-1 tert-butyl-(3-1,3-dithian-2-yl-propoxy)-dimethyl-silane 
• 606926-17-4 1-chloromethyl-2-dimethoxymethyl-3,5-dimethoxybenzene 
• 705-76-0 3,5-dimethoxybenzyl alcohol 
• 166322-67-4 2-(chloromethyl)-4,6-dimethoxy-benzaldehyde 
• 53178-48-6 2-(3'-hydroxypropyl)-1,3-dithiane 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 606926-19-6 tert-butyl-{3-[2-(2-dimethoxymethyl-3,5-dimethoxy-4-methylbenzyl)-[1,3]dithian-2-yl]propoxy}dimethylsilane 
• 606926-26-5 6-[5-(tert-butyldimethylsilyloxy)-1-(4-methoxybenzyl)-2-oxopentyl]-2,4-dimethoxy-3-methylbenzaldehyde 
• 606926-25-4 6-[1-benzyl-5-(tert-butyldimethylsilyloxy)-2-oxopentyl]-2,4-dimethoxy-3-methylbenzaldehyde 
• 606926-20-9 6-{2-[3-(tert-butyldimethylsilyloxy)propyl]-[1,3]dithian-2-ylmethyl}-2,4-dimethoxy-3-methylbenzaldehyde 
• 853247-26-4 acetic acid 3-(3-acetoxypropyl)-2-benzyl-5-chloro-7-methyl-6,8-dioxo-2,6,7,8-tetrahydroisoquinolin-7-yl ester 
• 853247-16-2 acetic acid 3-[2-(2-formyl-3,5-dimethoxy-4-methylbenzyl)[1,3]dithian-2-yl]propyl ester 
• 853247-19-5 acetic acid 5-(2-chloro-6-formyl-3,5-dihydroxy-4-methylphenyl)-4-oxopentyl ester 
• 853247-15-1 6-[2-(3-hydroxypropyl)[1,3]dithian-2-ylmethyl]-2,4-dimethoxy-3-methylbenzaldehyde 
• 853247-17-3 acetic acid 5-(2-formyl-3,5-dimethoxy-4-methylphenyl)-4-oxopentyl ester 
• 853247-18-4 acetic acid 5-(2-formyl-3,5-dihydroxy-4-methylphenyl)-4-oxopentyl ester 

Relevant academic research and scientific papers

Synthesis studies toward chloroazaphilone and vinylogous γ-pyridones: Two common natural product core structures

Chloroazaphilone is a common structure found in a number of natural products. Reported herein is a practical synthesis of a model chloroazaphilone that utilizes Pb(OAc)4 oxidation of HClO4/ HOAc pyrinium salt in a key one-pot operati

A practical procedure for multisubstituted β-naphthols and their derivatives

A number of multisubstituted β-naphthols were efficiently prepared by intramolecular aldol condensation of readily available substituted benzyaldehydes, whose substituents were introduced easily by a selective alkylation on the benzylic position of the su