55001-06-4

Upstream product

• 62751-30-8 (E)-ethyl 4-methyl-3-phenylpent-2-enoate 
• 107202-86-8 5-methyl-4-phenylhexanenitrile 
• 72277-17-9 (+/-)-ethyl 4-methyl-3-phenylpentanoate 
• 611-70-1 phenyl isopropyl ketone 
• 71-43-2 benzene 
• 55001-04-2 (+/-)-4-methyl-3-phenyl-1-pentanol 
• 51690-50-7 4-methyl-3-phenylpentanoic acid 
• 83303-62-2 1-Diazo-5-methyl-4-phenyl-hexan-2-one 
• 124-38-9 carbon dioxide 
• 55001-05-3 [1-(2-Bromo-ethyl)-2-methyl-propyl]-benzene 

Relevant academic research and scientific papers

Enantioselective halogenative semi-pinacol rearrangement: A stereodivergent reaction on a racemic mixture

An efficient, quantitative deracemization strategy for optically inactive allylic cycloalkanols has been achieved using the biphasic halogenative semi-pinacol reaction protocol. The resultant β-halo spiroketones, containing three contiguous stereogenic ce

Synthese de methoxycarbonylindenes, dihydro-1,2 naphtalenes et benzocycloheptene. Obtention des indanones-1, des tetralones-1 et de la benzosuberone correspondantes

The synthesis of methoxycarbonylindenes, 1,2-dihydro-naphtalenes, and benzocycloheptene starting from the corresponding 1-indanones, 1-tetralones, and benzosuberone is reported.The starting ketones were synthesized by methods described in the literature which were optimized; in some cases new processes are described.