548490-58-0

Upstream product

• 67-56-1 methanol 
• 57096-11-4 N6-[[(2-Chlorophenyl)methoxy]carbonyl]-N2-[t-butyloxycarbonyl]-D-lysine 

Downstream Products

• 871815-64-4 (R)-2-[(S)-2-tert-Butoxycarbonylamino-6-(2-chloro-benzyloxycarbonylamino)-hexylamino]-6-(2-chloro-benzyloxycarbonylamino)-hexanoic acid methyl ester 
• 871815-70-2 (R)-2-[(S)-2-tert-Butoxycarbonylamino-6-(2-chloro-benzyloxycarbonylamino)-hexylamino]-6-(2-chloro-benzyloxycarbonylamino)-hexanoic acid 
• 871815-69-9 (R)-2-[(R)-2-tert-Butoxycarbonylamino-6-(2-chloro-benzyloxycarbonylamino)-hexylamino]-6-(2-chloro-benzyloxycarbonylamino)-hexanoic acid 
• 548490-54-6 2-(2-tert-butoxycarbonylamino-ethylamino)-6-(2-chloro-benzyloxycarbonylamino)-hexanoic acid 
• 548490-56-8 2-(2-tert-butoxycarbonylamino-ethylamino)-6-(2-chloro-benzyloxycarbonylamino)-hexanoic acid methyl ester 
• 871815-63-3 (R)-2-[(R)-2-tert-Butoxycarbonylamino-6-(2-chloro-benzyloxycarbonylamino)-hexylamino]-6-(2-chloro-benzyloxycarbonylamino)-hexanoic acid methyl ester 

Relevant academic research and scientific papers

Synthesis of new chiral PNAs bearing a dipeptide-mimic monomer with two lysine-derived stereogenic centres

The synthesis of new chiral PNA analogues based on lysine is reported. In particular, l- and/or d-lysine-based PNA submonomers bearing two lysine side chains exactly spaced as in the dipeptide Lys-Lys were synthesized and incorporated in the middle of dec

Fast, solid-phase synthesis of chiral peptide nucleic acids with a high optical purity by a submonomeric strategy

The solid-phase synthesis of chiral peptide nucleic acids (PNAs) usually results in partial epimerization of the products, since the α-nitrogen atom of the amino acid is involved in an amidic bond. It is also time-consuming, since all the chiral monomers