817618-10-3

Upstream product

• 944275-72-3 C₁₀H₈BrN₃O₂ 
• 106-37-6 1.4-dibromobenzene 
• 4538-50-5 methyl (2S)-glycidate 

Downstream Products

• 869090-09-5 methyl (S)-3-(4-bromophenyl)-2-(cyclopropylmethoxy)propanoate 
• 869090-19-7 methyl (S)-2-benzyloxy-3-[3'-(3-heptyl-1-methylureido)biphenyl-4-yl]propanoate 
• 869090-13-1 methyl (S)-3-(4-bromophenyl)-2-(propyloxy)propanoate 
• 869090-17-5 methyl (S)-3-(4-bromophenyl)-2-benzyloxypropanoate 
• 817618-11-4 methyl 3-(4-bromophenyl)-2(S)-ethoxypropanoate 

Relevant academic research and scientific papers

Asymmetric transfer hydrogenation of α-azido acrylates

The asymmetric transfer hydrogenation of α-azido acrylates has been explored, a range of α-hydroxy esters are produced with good enantioselectivities (80-90% ee). The reaction was conducted in the wet HCO2H/NEt3 with Ru-TsDPEN A.

NOVEL BIAROMATIC COMPOUNDS WHICH ACTIVATE PPARγ-TYPE RECEPTORS, THEIR PROCESS OF PREPARATION AND THEIR USE IN COSMETIC OR PHARMACEUTICAL COMPOSITIONS

The invention relates to novel biaromatic compounds which correspond to the following general formula (I) and to their method of preparation and to their use in pharmaceutical compositions intended for use in human or veterinary medicine, in particular in

NOVEL COMPOUNDS THAT MODULATE PPARγ TYPE RECEPTORS, AND USE THEREOF IN COSMETIC OR PHARMACEUTICAL COMPOSITIONS

The invention relates to novel compounds corresponding to the general formula (I) below: (I) and also to the method for preparing them, and to their use in pharmaceutical compositions intended for use in human or veterinary medicine (in dermatology, and also in the fields of cardiovascular diseases, immune diseases and/or diseases associated with lipid metabolism),-or alternatively in cosmetic compositions.