Synthesis of trans-Vitamin D2
| dc.contributor.author | Weeks, Cassandra | |
| dc.date.accessioned | 2026-02-23T20:36:19Z | |
| dc.date.available | 2026-02-23T20:36:19Z | |
| dc.date.issued | 3/8/2019 | |
| dc.description.abstract | The synthesis of the trans-vitamin D2, via its sulfur dioxide adduct, is presented here. The trans isomer of vitamin D2 will be used as a model molecule, for the study of the photo-sensitized photoisomerization of vitamin D2 from its trans isomer to the naturally occurring, biologically active, cis isomer. The photoisomerization study will help advance the synthesis of a cis-vitamin D5 intermediate, subject to a different, multistep synthesis of 1?-hydroxyvitamin D5, a cancer chemopreventive agent. The synthesized trans-vitamin D2 was purified by column chromatography and characterized by 1H-NMR spectrometry. The overall chemical yield was of 71%. | |
| dc.description.department | Northeastern State University | |
| dc.identifier.other | Mathematics and Science.Chemistry.09 | |
| dc.identifier.uri | https://shareok.org//handle/11244/342080 | |
| dc.relation.ispartofseries | Mathematics and Science | |
| dc.subject.keywords | Chemistry | |
| dc.title | Synthesis of trans-Vitamin D2 | |
| dc.type | Abstract |
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