96363-21-2

Upstream product

• 67-56-1 methanol 
• 96363-20-1 D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoic acid 
• 123-11-5 4-methoxy-benzaldehyde 
• 159990-12-2 (S)-3-tert-Butoxycarbonylamino-3-(4-methoxy-phenyl)-propionic acid 
• 74-88-4 methyl iodide 
• 159848-74-5 1,1-dimethylethyl (R)-N-[2-hydroxy-1-(4-methoxyphenyl)-ethyl]carbamate 
• 159848-75-6 (S)-3-(N-terc-butoxycarbonylamine)-3-(4-methoxyphenyl)propanenitrile 
• 159990-11-1 (R)-2-tert-butoxycarbonylamino-1-methanesulfonyloxy-2-(4-methoxyphenyl)ethane 
• 193073-85-7 methyl (R)-2-((tert-butoxycarbonyl)amino)-2-(4-methoxyphenyl)acetate 
• 131690-56-7 (S)-β-amino-β-(4-methoxyphenyl)propionic acid 
• 24424-99-5 di-tert-butyl dicarbonate 
• 131791-82-7 3-amino-3-(4-methoxyphenyl)propionic acid methyl ester 

Downstream Products

• 96363-22-3 D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)<1-2H>propanal 
• 96363-23-4 (1S)-D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)<1-2H>propanol 
• 96363-23-4 (1R)-D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)<1-2H>propanol 
• 96363-29-0 (1S)-D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)<1-2H>propyl propanoate 
• 96363-29-0 C₁₈H₂₆⁽²⁾HNO₅ 
• 96363-27-8 C₂₅H₃₀⁽²⁾HNO₇ 
• 96363-27-8 C₂₅H₃₀⁽²⁾HNO₇ 
• 159848-76-7 methyl (+)-(3S)-3-amino-3-(4-methoxyphenyl)propanoate 
• 159848-82-5 methyl (3S,3'S)-3-<3'-tert-butyldimethylsiloxy-3'-(4-methoxyphenyl)propylamino>-3-(4-methoxyphenyl)propionate 
• 159848-94-9 methyl (3S,3S')-3-<3'-tert-butoxycarbonylamino-3'-(4-methoxyphenyl)propylamino>-3-(4-methoxyphenyl)propionate 
• 159848-84-7 [(S)-3-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-phenyl)-propyl]-[(S)-3-hydroxy-1-(4-methoxy-phenyl)-propyl]-carbamic acid tert-butyl ester 
• 159848-96-1 (3S,3S')-3--3-(4-methoxyphenyl)-1-propanol 
• 159848-83-6 methyl (3S,3'S)-3--3-(4-methoxyphenyl)propionate 
• 159848-86-9 (3S,3'S)-3--3-(4-methoxyphenyl)-1-(2,2,2-trichloroethoxycarbonyloxy)propane 

Relevant academic research and scientific papers

Synthesis of macrocycles containing 1,3,4-oxadiazole and pyridine moieties

A series of peptide-like 25-28 membered macrocycles containing 1,3,4-oxadiazoles and pyridines bearing a chiral center scaffold have been synthesized by using known coupling reagents and common protecting groups. The yield of the purified macrocycles was poor on an average, yet it seems to be independent of amino acid substitution or stereochemistry. These macrocycles represent a new class of structures for further development and for future application in high-throughput screening against a variety of biological targets.

Total Synthesis of 2'-Deoxymugineic Acid and Nicotianamine

Steroselective total synthesis of the unique phytosiderophores, 2'-deoxymugineic acid (4) and nicotianamine (5), has been achieved from the β-tyrosine derivative 21 using its aryl groups as the carboxyl synthon.

Synthesis of (4R)-D,L-- and (4S)-D,L-Homoserine Lactones

The (4R)-D,L-- and (4S)-D,L-homoserine lactone hydrochloride salts were prepared from D,L-3-amino-3-(4-methoxyphenyl)propanoic acid (1) in eight steps in an overall yields of 5.0percent.Amino acid 1 was converted into D,L-3-(1,1-dimethyletho