252987-07-8Relevant articles and documents
Transformation of vitamin B6 to (+)-deoxypyridinoline, a useful biochemical marker for diagnosis of bone diseases
Adamczyk, MacIej,Akireddy, Srinivasa Rao,Reddy, Rajarathnam E.
, p. 2379 - 2390 (2007/10/03)
A versatile chiral synthesis of the cross-link (+)-deoxypyridinoline (Dpd, 2) was achieved starting from vitamin B6 (7). The key steps in the synthesis of (+)-2 are transformation of B6 (7) to the chloride (3d) and construction of three α-amino acid chains by utilizing (R)-(-)-Schollkopf's reagent (4), Wittig reagent (R)-(-)-5, and iodide (5)-(-)-6. (+)-Dpd (2) is a degradation product of bone collagen and has been found to be a useful marker for diagnosis of osteoporosis and other metabolic bone diseases. (C) 2000 Elsevier Science Ltd.
Versatile synthesis of (+)-deoxypyridinoline, a biochemical marker for diagnosis of osteoporosis
Adamczyk, Maciej,Rao Akireddy, Srinivasa,Reddy, Rajarathnam E.
, p. 3107 - 3110 (2007/10/03)
A versatile chiral synthesis of the bone collagen cross-link, (+)-deoxypyridinoline (Dpd, 1) was described starting from a 3-hydroxypyridine derivative (2) via sequential introduction of three amino acid chains followed by hydrolysis. The key synthon 2, was prepared from vitamin B6 (6).