313256-73-4

Upstream product

• 140-11-4 Benzyl acetate 
• 86983-92-8 (E)-4-methyl-1-(p-nitrophenyl)-1-penten-3-one 
• 261527-26-8 1-hydroxy-4-methyl-1-(4-nitrophenyl)pentan-3-one 
• 261527-27-9 1-acetoxy-4-methyl-1-(p-nitrophenyl)pentan-3-one 

Downstream Products

• 261527-36-0 3-[2-(p-aminophenyl)-ethyl]-3-hydroxy-4-methylpentanoic acid 

Relevant academic research and scientific papers

Methods of making dihydropyrone HIV protease inhibitors

The present invention relates to methods of making dihydropyrone HIV inhibitors.

Application of the Sch?pf method to optimization of the synthesis of 3-[2-(p-N-acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic acid: Simultaneous reduction of three functional groups to maximize yield and throughput

Application of the Sch?pf method to development of a high yield condensation process to prepare a labile β-(p-nitrophenyl)-α,β-unsaturated ketone system, along with development of a procedure for simultaneous hydrogenation/hydrogenolysis of olefin, benzyl