1262850-97-4

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 22862-76-6 (-)-anisomycin 
• 17355-24-7 methyl (R)-2-acetamido-3-(4-methoxyphenyl)propanoate 
• 19764-32-0 Ac-D-Tyrosine 
• 556-02-5 tyrosine 
• 1380403-20-2 C₁₄H₁₉NO₄ 
• 1380403-17-7 C₁₄H₁₉NO₃ 
• 1380403-14-4 C₁₄H₁₇NO₃ 
• 1380403-11-1 (R)-N-(1-(4-methoxyphenyl)-3-oxopropan-2-yl)acetamide 
• 1380403-08-6 C₁₂H₁₇NO₃ 
• 1380403-25-7 C₂₀H₃₁NO₉S 
• 1380403-23-5 C₁₉H₂₉NO₇ 
• 1380403-22-4 C₁₄H₁₇NO₃ 

Downstream Products

• 1262850-99-6 C₁₅H₁₇NO₆ 
• 1262850-98-5 C₁₅H₁₇NO₆ 
• 22862-76-6 (-)-anisomycin 

Relevant academic research and scientific papers

Concise synthesis of (-)-anisomycin

The antibiotic (-)-anisomycin was synthesized starting from d-tyrosine using Sharpless asymmetric epoxidation as a key reaction followed by formation and hydrolysis of oxazoline set up all chiral center.

Formal synthesis of AB3217-A from anisomycin using a directed benzylic oxidation

A formal synthesis of the insecticidal natural product AB3217-A involving an unusual diastereoselective benzylic oxidation is described.