313478-67-0

Upstream product

• 313478-65-8 Methyl (S)-2,2-dimethyl-3-[N-(2'-methoxy-6'-methylphenyl)-N-((S)-tert-leucyl)]amino-3-phenylpropionate 
• 50868-73-0 2-methoxy-6-methylbenzeneamine 
• 31469-15-5 1-methoxy-2-methyl-1-trimethylsiloxy-1-propene 
• 220892-32-0 Methyl (S)-2,2-dimethyl-3-phenyl-3-[N-(2'-methoxy-6'-methylphenyl)-N-((S)-N',N'-phthaloyl-tert-leucyl)]aminopropionate 
• 220892-42-2 (E)-2-methoxy-6-methyl-N-(phenylmethylene)benzeneamine 
• 100-52-7 benzaldehyde 

Relevant academic research and scientific papers

Asymmetric steering of the Mannich reaction with phthaloyl amino acids

Mannich-type reactions are powerful methods for the efficient synthesis of β-amino carbonyl compounds that are valuable intermediates for the construction of natural products, β-peptides, and peptidomimetics. For the efficient steric steering of Mannich r