765910-61-0

Upstream product

• 2426-87-1 3-methoxy-4-(phenylmethoxy)benzaldehyde 
• 1730-25-2 allylmagnesium bromide 
• 121-33-5 vanillin 
• 106-95-6 allyl bromide 

Downstream Products

• 1426433-79-5 1-(4-benzyloxy-3-methoxyphenyl)butan-1,4-diol 
• 1426433-78-4 1-(4-hydroxy-3-methoxyphenyl)butan-1,4-diol 
• 1449790-27-5 2-[4-(benzyloxy)-3-methoxyphenyl]-2,3,4,5-tetrahydro-1-benzoxepine 
• 1449789-99-4 1-[4-(benzyloxy)-3-methoxyphenyl]-4-(2-bromophenyl)butan-1-ol 
• 1449789-89-2 C₂₄H₂₃BrO₃ 
• 880262-23-7 2-[2-[4-(benzyloxy)-3-methoxyphenyl]-2-(prop-2-ynyloxy)ethyl]oxirane 

Relevant academic research and scientific papers

Diastereoselective synthesis of 5-hydroxy-8-methoxy-1-oxaspiro[5,5]undeca- 7,10-diene-9-one

A short five steps synthesis of the title compound from vanillin is described. The racemic spiroether 7 was obtained in 61% yield and in >99% diastereomeric excess (by 1H-NMR) from the corresponding phenolic derivative 3 by oxidation with lead (IV) acetate.

Transition metals catalyzed C-C and C-O bonds formation: Facile synthesis of flavans and benzoxepines

A simple and practical method has been developed based on intermolecular [Pd]-catalyzed C-C and an intramolecular [Cu]-catalyzed C-O bond formations for the synthesis of flavans and benzoxepines. Interestingly, the method is amenable for the synthesis of

Mild and efficient allylation of aldehydes mediated by titanium(III) chloride

A mild, chemoselective and efficient method for the allylation of aldehydes is described. Ketones remained unreacted under the reaction conditions.