59276-32-3

Upstream product

• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 
• 77-78-1 dimethyl sulfate 
• 77-76-9 2,2-dimethoxy-propane 
• 86-51-1 2,3-dimethyoxybenzaldehyde 
• 67-56-1 methanol 

Downstream Products

• 134451-75-5 (2R,5R,6S)-(E)-methyl 6-(2,3-dimethoxyphenyl)-6-methoxy-2,5-dimethylhex-3-enoate 
• 134333-55-4 (2R,5R,6S)-(E)-methyl 6-(2,3-dimethoxyphenyl)-2,6-dimethoxy-5-methylhex-3-enoate 
• 134333-57-6 (2R,5S,6R)-(E)-methyl 6-(2,3-dimethoxyphenyl)-6-methoxy-2,5-dimethylhex-3-enoate 
• 5150-42-5 2,3-dimethoxyphenol 
• 2150-42-7 methyl 2,3-dimethoxybenzoate 
• 92720-69-9 (2,3-Dimethoxy-phenyl)-methoxy-methyl-hydroperoxide 

Relevant academic research and scientific papers

1,3-Oxazolidin-5-ones derived from proline as chiral components in the synthesis of predictive enantioselective coupling reagents

1,3-Oxazolidin-5-ones derived from both enantiomers of proline and trichloroacetaldehyde were prepared and applied as an amine component in the synthesis of chiral predictive triazine-based coupling reagents. The reagents were found to be useful in condensations yielding enantiomerically enriched products from racemic substrates.

Ru(II)-functionalized SBA-15 as highly chemoselective, acid free and sustainable heterogeneous catalyst for acetalization of aldehydes and ketones

Combining electron deficient Ru(II) coordination sites with organofunctionalized SBA-15, (L)Ru(II)@SBA-15, result in a mild, neutral, water scavenger free and chemo-selective acetalization catalyst for cyclic/acyclic acetals. Vacant coordination sites of ruthenium in (L)Ru(II)@SBA-15 activates protecting groups as well as reactants simultaneously and restricts the reverse acetalization reaction. Synthesized (L)Ru(II)@SBA-15 catalyst has been thoroughly characterized and act as competitive catalyst compared to conventional acid catalysts. (L)Ru(II)@SBA-15 performs high catalytic activity as well as selectivity within 20 min with high TOF. The catalyst can be recycled and reaction parameters are optimized.