104554-87-2

Upstream product

• 4392-24-9 Cinnamyl bromide 
• 104554-86-1 (+)-3-(5-Phenyl-2(R)-methyl-1-oxo-4(E)-pentenyl)-4(S)-isopropyl-1,3-oxazolidin-2-one 
• 128329-60-2 Methanesulfonic acid (E)-(R)-2-methyl-5-phenyl-pent-4-enyl ester 
• 73407-97-3 (2R,4E)-2-methyl-5-phenyl-4-penten-1-ol 

Downstream Products

• 128329-62-4 (4R,1E)-4,6-dimethyl-7-((1,1-dimethylethenyl)diphenylsiloxy)-1-phenyl-1-heptene 
• 104554-89-4 (4R,6E)-2,4-dimethyl-7-phenyl-6-heptenoic acid 
• 128329-61-3 (4R,6E)-2,4-dimethyl-7-phenyl-6-hepten-1-ol 
• 104554-88-3 (2S,4'R,6'E)-1-(2',4'-dimethyl-7'-phenyl-6'-heptenoyl)-2-(hydroxymethyl)pyrrolidine 

Relevant academic research and scientific papers

TOTAL SYNTHESIS OF THE IONOPHORE ANTIBIOTIC IONOMYCIN. ASYMMETRIC SYNTHESIS OF THE C1-C10 AND C11-C16 SYNTHONS.

Asymmetric synthesis of the synthons 1 and 3 are described.Absolute stereochemical relationships in these intermediates have been established via chiral enolate and directed hydrogenation processes.