161009-60-5

Upstream product

• 97-51-8 5-Nitrosalicylaldehyde 
• 39224-61-8 2-hydroxy-5-nitrobenzyl alcohol 
• 161009-58-1 [2-(2-Methoxy-ethoxymethoxy)-5-nitro-phenyl]-methanol 

Downstream Products

• 161009-70-7 (S)-3-[5-tert-Butoxycarbonylamino-2-(2-methoxy-ethoxymethoxy)-benzyloxy]-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid methyl ester 
• 161009-68-3 (S)-3-[5-tert-Butoxycarbonylamino-2-(2-methoxy-ethoxymethoxy)-benzyloxy]-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid 
• 161009-64-9 (S)-3-[5-tert-Butoxycarbonylamino-2-(2-methoxy-ethoxymethoxy)-benzyloxy]-2-(trityl-amino)-propionic acid methyl ester 
• 161009-66-1 (S)-2-Amino-3-[5-tert-butoxycarbonylamino-2-(2-methoxy-ethoxymethoxy)-benzyloxy]-propionic acid methyl ester 
• 161009-62-7 (S)-3-[2-(2-Methoxy-ethoxymethoxy)-5-nitro-benzyloxy]-2-(trityl-amino)-propionic acid methyl ester 

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.