29128-53-8

Upstream product

• 854869-30-0 1-acetoxy-1-(3,4-dimethoxy-phenyl)-2-nitro-propane 
• 855273-11-9 1-acetoxy-1-(4-benzyloxy-3-methoxy-phenyl)-2-nitro-propane 
• 103502-07-4 1-(3,4-dimethoxy-phenyl)-propane-1,2-dione-2-oxime 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 6309-18-8 2-(3,4-dimethoxyphenyl)-2-hydroxyacetonitrile 
• 95392-01-1 2-(3,4-dimethoxyphenyl)-2-((trimethylsilyl)oxy)acetonitrile 
• 186581-53-3 diazomethane 
• 10317-28-9 (1RS,2SR)-2-amino-1-(4-hydroxy-3-methoxy-phenyl)-propan-1-ol 
• 74812-63-8 dl-nordefrin 
• 10317-28-9 threo-2-amino-1-(4-hydroxy-3-methoxy-phenyl)-propanol-⁽¹⁾ 
• 90253-98-8 2-Amino-1-(3,4-dimethoxyphenyl)-1-propanon-hydrochlorid 
• 40513-44-8 2-amino-1-(3,4-dimethoxy-phenyl)-propan-1-one 

Downstream Products

• 70664-06-1 5-(3,4-dimethoxyphenyl)-4-methyl-2-oxazolidinone 
• 90253-96-6 2-(Acetylamino)-1-(3,4-dimethoxyphenyl)-1-propanon 
• 860746-60-7 N-[2-(3,4-Dimethoxy-phenyl)-2-hydroxy-1-methyl-ethyl]-acetamide 

Relevant academic research and scientific papers

Applications of Optically Active Aryl Cyanohydrins in the Synthesis of α-Hydroxy Aldehydes, α-Hydroxy Ketones and β-Hydroxy Amines

Cyanohydrins, prepared in high optical purity from aryl aldehydes, have been converted into α-hydroxy aldehydes, α-hydroxy ketones and β-hydroxy amines without any racemization and frequently with good stereoselectivity for the erythro-diastereoisomer (>90percent) at the newly introduced stereogenic centre.

5-(Substituted phenyl)-oxazolidinones and their sulfur analogs

Novel 5-(substituted phenyl)-oxazolidinones and their sulfur analogs of Formula I STR1 wherein R1 is optionally substituted lower alkyl, cycloalkyl or cycloalkylalkyl; R2 is hydrogen, optionally substituted lower alkyl, cycloalkyl, c