1569905-46-9

Upstream product

• 615-37-2 ortho-methylphenyl iodide 
• 292638-85-8 acrylic acid methyl ester 
• 109-64-8 1,3-dibromo-propane 

Downstream Products

• 1569905-56-1 methyl (2E)-3-[2-(3-{bis[(tert-butoxy)carbonyl]amino}propyl)-6-methylphenyl]prop-2-enoate 
• 1569905-83-4 tert-butyl N-[3-(2-{3-[(4R)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]-3-oxopropyl}-3-methylphenyl)propyl]carbamate 
• 1569905-65-2 C₁₈H₂₇NO₄ 
• 1569905-91-4 benzyl (2R)-3-[2-(3-{[(tert-butoxy)carbonyl]amino}propyl)-6-methylphenyl]-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoate 
• 1569905-74-3 tert-butyl N-[3-(2-{3-[(4R)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]-3-oxopropyl}-3-methylphenyl)propyl]carbamate 

Relevant academic research and scientific papers

A palladium-catalyzed domino reaction as key step for the synthesis of functionalized aromatic amino acids

A variety of substituted aromatic systems are synthesized by the Catellani reaction. These are used as precursors for novel amino acids with a basic side chain. Georg Thieme Verlag Stuttgart New York.