309928-91-4

Upstream product

• 58456-27-2 (S)-3-(benzyloxycarbonyl)-4-(4-diazo-3-oxobutyl)-5-oxazolidinone 
• 495401-21-3 tert-butyl (2S)-2-benzyloxycarbonylamino-6-bromo-5-hydroxyhexanoate 
• 204074-52-2 tert-butyl 2-benzyloxycarbonylamino-4-(2-oxiranyl)butanoate 
• 495401-22-4 (2S,5S)-2-benzyloxycarbonylamino-5-bromomethyl-δ-valerolactone 
• 112157-39-8 Nα-(Benzyloxycarbonyl)-L-lysine tert-butyl ester 
• 127623-77-2 tert-butyl (S)-2-benzyloxycarbonylamino-6-hydroxyhex-5-enoate 
• 495401-24-6 methyl (2S,5S)-2-benzyloxycarbonylamino-6-bromo-5-hydroxyhexanoate 
• 15366-19-5 methyl (S)-2-benzyloxycarbonylamino-6-diazo-5-oxohexanoate 

Downstream Products

• 309928-96-9 (2S,5R)-6-azido-2-benzyloxycarbonylamino-5-hydroxyhexanoic acid 
• 309928-97-0 (2S,5S)-6-azido-2-benzyloxycarbonylamino-5-hydroxyhexanoic acid 
• 309928-94-7 (2S,5R)-5-azidomethyl-2-benzyloxycarbonylamino-δ-valerolactone 
• 309928-95-8 (2S,5S)-5-azidomethyl-2-benzyloxycarbonylamino-δ-valerolactone 
• 504-91-6 (5R)-5-hydroxy-L-lysine 
• 18899-29-1 (2S,5S)-5-hydroxylysine 
• 495401-24-6 methyl (2S,5S)-2-benzyloxycarbonylamino-6-bromo-5-hydroxyhexanoate 
• 309928-92-5 methyl (S)-6-azido-2-benzyloxycarbonylamino-5-oxohexanoate 

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.

Synthesis of all four possible stereoisomers of 5-hydroxylysine

A simple protocol for the transformation of L- and D-glutamic acids into the enantiopure forms of all four isomers of 5-hydroxylysine is described. Copyright (C) 2000 Elsevier Science Ltd.