42600-75-9

Upstream product

• 3282-30-2 pivaloyl chloride 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 

Downstream Products

• 134699-80-2 2-(3,4-Dimethoxy-phenyl)-3-(2,2-dimethyl-propionylamino)-propionic acid 
• 81254-99-1 1-(tert-butyl)-6,7-dimethoxy-3,4-dihydroisoquinoline 
• 91361-03-4 N-<2-(2-Chlor-4,5-dimethoxyphenyl)-ethyl>-2,2-dimethylpropionsaeureamid 
• 85362-72-7 N-<2-(3,4-Dimethoxyphenyl)-ethyl>-2,2-dimethylpropionsaeureimidchlorid Hydrochlorid 
• 29539-03-5 5,6-dihydroxy-indoline 
• 91361-04-5 N-<2-(2-Brom-4,5-dimethoxyphenyl)-ethyl>-2,2-dimethylpropionsaeureamid 
• 42600-74-8 N-(3,4-dihydroxyphenethyl)pivalamide 
• 91248-23-6 3-Amino-2-(3,4-dimethoxy-phenyl)-propionic acid; hydrochloride 
• 344336-76-1 N-<2-(3,4-Dimethoxyphenyl)-ethyl>-2,2-dimethylpropionsaeureimidchlorid 

Relevant academic research and scientific papers

Iridium-Catalyzed Asymmetric Hydrogenation of Sterically Hindered Cyclic Imines for Enantioselective Synthesis of Tetrahydroisoquinolines

An efficient enantioselective hydrogenation of sterically hindered cyclic imines catalyzed by the Ir-tBu-ax-Josiphos complex has been described, producing a series of useful chiral bulky tetrahydroisoquinoline analogs in high isolated yields (85-96%) with good to excellent enantioselectivities (74-99% ee). This transformation provided highly straightforward access to the useful derivatives of tetrahydroisoquinolines, which are of great potential value in drug molecule and natural product research.

Preparation method of compound 5,6-dihydroxy indoline and halogen acid salts thereof

The invention relates to a preparation method of a compound 5,6-dihydroxy indoline and halogen acid salts thereof. Phenylethylamine SM-0 sold in the market is used as a raw material and firstly reactswith acyl chloride to obtain amide SM-1; amide SM-1 rea

Substituted aryl and aralkyl amides in the treatment of parkinsonism

Amides having aromatic substituents of the formula: SPC1 Wherein R is an acyl radical derived from a carboxylic acid having from 3 to 20 carbon atoms, X and Y are members selected from the group consisting of hydrogen, fluoro, trifluoromethyl and hydroxy, and n is an integer selected from the group consisting of 0, 1 and 2, exhibit an effect upon the central nervous system.