88492-29-9

Usage

InChI:InChI=1/C8H16N2O4/c1-6(11)10(14)5-3-2-4-7(9)8(12)13/h7,14H,2-5,9H2,1H3,(H,12,13)/t7-/m0/s1

Upstream product

• 112157-44-5 N^ε-Acetyl-N^ε-hydroxy-N^α-(carbobenzyloxy)-L-lysine 
• 2212-75-1 N₂-[(benzyloxy)carbonyl]-L-lysine 
• 26348-68-5 N-(benzyloxycarbonyl)lysine methyl ester hydrochloride 
• 157505-72-1 (S)-2-Benzyloxycarbonylamino-6-hydroxyamino-hexanoic acid methyl ester 
• 157505-71-0 C₁₈H₂₆N₂O₅ 
• 112157-40-1 (S)-6-(Acetyl-benzoyloxy-amino)-2-benzyloxycarbonylamino-hexanoic acid tert-butyl ester 
• 112157-43-4 N⁶-acetyl-N²-benzyloxycarbonyl-N⁶-L-hydroxylysine tert-butyl ester 
• 157505-73-2 N^ε-Acetyl-N^ε-hydroxy-N^α-(carbobenzyloxy)-L-lysine methyl ester 

Relevant academic research and scientific papers

A New Method for the Synthesis of Nε-Acetyl-Nε-hydroxy-L-lysine, the Iron-Binding Constituent of Several Important Siderophores

Oxidation of the ε-amino group of Nα-(carbobenzyloxy)-L-lysine methyl ester with dimethyldioxirane in acetone gave the acetone-derived nitrone of the desired hydroxylamine.Acidic hydrolysis, acetylation, and subsequent deprotection provided a s

OXIDATION OF AMINO ACID. PART V. A NOVEL SYNTHESIS OF N6-ACETYL-N6-HYDROXYLYSINE FROM LYSINE

N6-Acetyl-N6-L-hydroxylysine was synthesized from L-lysine by oxidation of the amino group in the N2-benzyloxycarbonyl-L-lysine tert-butyl ester with benzoyl peroxide and subsequent acetylation.