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1 used to construct the dienyne precursors of previtamin 6 possessing two methyl groups capable of par
2 nalyzed in depth, i.e., the conformations of previtamin D and the quantum effects associated with the
3 e characterization of the conformers of both previtamin D and vitamin D allowed the calculation of th
4 analogue 12 was prone to conversion into its previtamin D form by thermal equilibration, the correspo
5 or-1alpha,25-(OH)2D3, were obtained from the previtamin D precursors, constructed by either Suzuki-Mi
7 he thermal isomerization reaction converting previtamin D to vitamin D is an intramolecular [1,7]-sig
9 ) was the most abundant product, followed by previtamin D(2), lumisterol(2) and tachysterol(2) in ord
10 study, the ergosterol-derived photoproducts previtamin D(2), lumisterol(2) and tachysterol(2) were,
14 at the conversion of 7-dehydrocholesterol to previtamin D3 was reduced in children a mean of 14 month
15 n the skin, leading to its transformation to previtamin D3, which is rapidly converted to vitamin D3.
16 sterification of the 3beta-hydroxy of preD3 (previtamin D3-3beta-acetate) reduced the rate of the iso
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