161009-67-2

Upstream product

• 161009-59-2 5-((2-methoxy)ethoxymethoxy)-2-nitrophenylmethanol 
• 60463-12-9 3-hydroxymethyl-4-nitrophenol 
• 161009-65-0 (S)-3-[2-tert-Butoxycarbonylamino-5-(2-methoxy-ethoxymethoxy)-benzyloxy]-2-(trityl-amino)-propionic acid methyl ester 
• 161009-63-8 (S)-3-[5-(2-Methoxy-ethoxymethoxy)-2-nitro-benzyloxy]-2-(trityl-amino)-propionic acid methyl ester 
• 161009-61-6 2-Iodomethyl-4-(2-methoxy-ethoxymethoxy)-1-nitro-benzene 

Downstream Products

• 161009-71-8 (S)-3-[2-tert-Butoxycarbonylamino-5-(2-methoxy-ethoxymethoxy)-benzyloxy]-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid methyl ester 
• 161009-69-4 (S)-3-[2-tert-Butoxycarbonylamino-5-(2-methoxy-ethoxymethoxy)-benzyloxy]-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid 

Relevant academic research and scientific papers

Synthesis of N-protected serine ethers as precursors of new photoactivatable amino acids cleavable by hydrogenolysis

Fmoc-(L)-serine ethers bearing either 2-(2'-methoxyethoxymerhyl ether)-5-terbutyloxycarbonylaminobenzyl (ortho) or 5-(2'-methoxyethoxymethy] ether)-2-terbutyloxycarbonylaminobenzyl (metal moieties were synthesized. Spectral characteristics of the corresponding photoactivatable 4-diazocyclohexa-2,5-dienones were determined.