73809-41-3Relevant articles and documents
Synthesis, conformational analysis, and biological-activity of the 1-α,25-dihydroxy-10,19-dihydrovitamin D3 isomers
Sicinski,Deluca
, p. 150 - 171 (2007/10/02)
The synthesis of the four 1α,25-dihydroxy-10,19-dihydrovitamin D3 stereoisomers (8-11) is described starting from 25-hydroxyvitamin D3(1c). Acetic acid-catalyzed cycloreversion of 1 α-hydroxylated 3,5-cyclovitamin D compound 14, prod
Direct C(1) Hydroxylation of Vitamin D3 and Related Compounds
Paaren, Herbert E.,DeLuca, Hector F.,Schnoes, Heinrich K.
, p. 3253 - 3258 (2007/10/02)
A direct synthesis of C(1) hydroxylated vitamin D analogues from the corresponding vitamin D precursors has been developed.Allylic oxidation of 3,5-cyclovitamin D derivatives, readily obtained from the buffered solvolysis of vitamin D tosylates, with selenium dioxide yields 1α-hydroxylated 3,5-cyclovitamin D compounds which are smoothly converted to the desired 1α-hydroxyvitamin D derivatives by acid-catalyzed cycloreversion.Application of this scheme to vitamin D3 (1a), 25-hydroxyvitamin D3 (1b), and vitamin D2 (1c) affords the 1α-hydroxy products in ca.20 percent overall yield.