189007-62-3

Upstream product

• 28252-50-8 N^α-Cbz-N^γ-(4,4'-dimethoxybenzhydryl)-Asn-OH 

Downstream Products

• 178361-86-9 (S)-2-Amino-N-[bis-(4-methoxy-phenyl)-methyl]-succinamic acid 2-trimethylsilanyl-ethyl ester 
• 178361-84-7 C₅₃H₆₆FN₇O₁₅ 
• 189007-66-7 (S)-N-[Bis-(4-methoxy-phenyl)-methyl]-2-[(2R,3R)-2-[(R)-2-(tert-butoxycarbonyl-methyl-amino)-4-methyl-pentanoylamino]-3-(4-fluoro-3-nitro-phenyl)-3-hydroxy-propionylamino]-succinamic acid 2-trimethylsilanyl-ethyl ester 
• 178361-88-1 (S)-N-[Bis-(4-methoxy-phenyl)-methyl]-2-[(2R,3R)-2-[(R)-2-(tert-butoxycarbonyl-methyl-amino)-4-methyl-pentanoylamino]-3-(4-fluoro-3-nitro-phenyl)-3-hydroxy-propionylamino]-succinamic acid 
• 189007-65-6 (S)-2-[(2R,3R)-2-Azido-3-(4-fluoro-3-nitro-phenyl)-3-hydroxy-propionylamino]-N-[bis-(4-methoxy-phenyl)-methyl]-succinamic acid 2-trimethylsilanyl-ethyl ester 
• 178361-87-0 (S)-2-[(2R,3R)-2-Amino-3-(4-fluoro-3-nitro-phenyl)-3-hydroxy-propionylamino]-N-[bis-(4-methoxy-phenyl)-methyl]-succinamic acid 2-trimethylsilanyl-ethyl ester 

Relevant academic research and scientific papers

Synthesis of the orienticin C M(2-4) macrocycle utilizing a nucleophilic aromatic substitution strategy

The synthesis of the fully functionalized M(2-4) macrocyclic orienticin C subunit 5 is described utilizing an intramolecular nucleophilic aromatic substitution reaction.