59276-36-7

Upstream product

• 149-73-5 trimethyl orthoformate 
• 212914-85-7 isovanilin 
• 621-59-0 isovanillin 

Downstream Products

• 811819-63-3 3-benzyloxy-2-iodo-4-methoxybenzoic acid 
• 811819-72-4 7-benzyloxy-8-methoxy-12-methyl-12-aza-benzo[h]spiro[5.6]dodec-1-ene-3,11-dione 
• 811819-69-9 9-benzyloxy-10-methoxy-14-methyl-1,4-dioxa-14-aza-benzo[j]dispiro[4.2.6.2]hexadec-6-en-13-one 
• 811819-66-6 3-benzyloxy-N-[2-(1,4-dioxaspiro[4,5]dec-7-en-8-yl)ethyl]-2-iodo-4-methoxy-N-methyl-benzamide 
• 138490-94-5 2-iodoisovanillin 
• 916225-90-6 2-iodo-4-methoxy-3-(methoxymethoxy)-1-(dimethoxymethyl)benzene 
• 151726-42-0 3-(benzyloxy)-2-iodo-4-methoxybenzaldehyde 
• 113275-17-5 (4-methoxy-3-(4-(methoxycarbonyl)phenoxy)benzyl)-triphenylphosphonium bromide 
• 113275-15-3 Methyl 4-<5-(hydroxymethyl)-2-methoxyphenoxy>benzoate 
• 113275-16-4 4-(5-Bromomethyl-2-methoxy-phenoxy)-benzoic acid methyl ester 
• 213264-64-3 3-methoxycarbonyl-5-{2-[4-(2-methoxy-5-dimethoxymethylphenoxy)phenyl]-ethyl}isoxazole 
• 213264-63-2 3-methoxycarbonyl-5-{2-[4-(2-methoxy-5-dimethoxymethylphenoxy)phenyl]-ethenyl}isoxazole 
• 213264-65-4 (5-{2-[4-(5-Dimethoxymethyl-2-methoxy-phenoxy)-phenyl]-ethyl}-isoxazol-3-yl)-methanol 
• 213264-66-5 3-{4-[2-(3-Bromomethyl-isoxazol-5-yl)-ethyl]-phenoxy}-4-methoxy-benzaldehyde 

Relevant academic research and scientific papers

Intramolecular Heck cyclization to the galanthamine-type alkaloids: Total synthesis of (±)-lycoramine

A novel approach towards the construction of the galanthamine skeleton was demonstrated by the total synthesis of (±)-lycoramine. The key steps include a Pd-catalyzed intramolecular cyclization to form the seven-membered azepane ring and a spontaneous int

Oxidation of o-Methoxyphenols with a Hypervalent Iodine Reagent: Improved Synthesis of Asatone and Demethoxyasatone

Oxidation of the 2-methoxyphenols 1c-f with phenyliodonium(III) diacetate (PIDA) in methanol resulted in the formation of the cyclohexa-2,4-dienones 4c-f, which dimerized spontaneously to a single product (5c-f) in each case. Using this method the synthes