495401-22-4

Upstream product

• 204074-52-2 tert-butyl 2-benzyloxycarbonylamino-4-(2-oxiranyl)butanoate 
• 112157-39-8 Nα-(Benzyloxycarbonyl)-L-lysine tert-butyl ester 
• 127623-77-2 tert-butyl (S)-2-benzyloxycarbonylamino-6-hydroxyhex-5-enoate 
• 495401-21-3 tert-butyl (2S)-2-benzyloxycarbonylamino-6-bromo-5-hydroxyhexanoate 

Downstream Products

• 309928-91-4 methyl (2S)-2-benzyloxycarbonylamino-6-bromo-5-oxohexanoate 
• 309928-95-8 (2S,5S)-5-azidomethyl-2-benzyloxycarbonylamino-δ-valerolactone 
• 495401-24-6 methyl (2S,5S)-2-benzyloxycarbonylamino-6-bromo-5-hydroxyhexanoate 

Relevant academic research and scientific papers

A simple and convenient transformation of L-lysine into pyridinoline and deoxypyridinoline, two collagen cross-links of biochemical interest

Starting from L-lysine as the only chiral building block, pyridinoline and deoxypyridinoline are efficiently synthesised, thus mimicking the postranscriptional formation of these collagen cross-links.