Canadian Journal of Chemistry p. 942 - 948 (1997)
Update date:2022-08-29
Topics:
Wolf, Eckardt
Kennedy, Isaac A.
Himmeldirk, Klaus
Spenser, Ian D.
New synthesis are described of 5-hydroxypentane-2,3-dione (7) (i.e., laurencione (7 ? 8)) and of 3-amino-1-hydroxypropan-2-one (3-amino-1- hydroxyacetone) (5) hydrochloride, putative precursors of the C5 unit, C- 2',2,3,4,4', and of the C3N unit, N-1,C-6,5,5', respectively, of pyridoxine (6). The condensation of hydroxypentane dione (i.e., laurencione) and aminohydroxypropanone forms a vitamin B, pyridoxine. The two compounds incorporated structural modifications on the formation mechanism of vitamin B. These compounds were considered as putative precursors of the C5 unit and the C3N unit of pyridoxine.
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