Abstract

AbstractThe purpose of this research experiment was to perform and improve the synthesis of resveratrol (CAS: 501-36-0). Resveratrol (trans-3,4',5-trihydroxystilbene), a natural polyphenolic, non-flavonoid antioxidant, is a phytoalexin found naturally in many plants. The compound was synthesized using the decarbonylative Heck reaction. The modified four-step reaction generated poor yields but the spectra indicate that the overall resveratrol compound was obtained. Several improvements were made to help increase yield.

Highlights

  • For many past centuries man has been in search of an elixir

  • Resveratrol has been able to extend the life of Saccharomyces cerevisiae,6 Caenorhabditis elegans, Drosophila melanogaster, 7 and the mammal

  • The second trial had a more accurate melting point that ranged from 89-­‐95 °C

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Summary

A Senior Paper

In Partial Fulfillment of the Requirements for the Degree of BACHELOR OF SCIENCE. iii Figure 17: The IR of Resveratrol Triacetate, product of step 3.

INTRODUCTION
Principles
RESULTS AND DISCUSSION
12 Figure 8
18 Figure 15
CONCLUSION
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