*Corresponding author:
Keti Zeka, National Health Service Blood and transplant, Department of Haematology, University of Cambridge, Cambridge CB2 0PT, UKReceived: June 20, 2018; Published: July 05, 2018
DOI: 10.26717/BJSTR.2018.06.001339
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Resveratrol is a well notorious compound that may play a role in the prevention of diabetes complications and different cancers. Along, resveratrol, a naturally occurring phytoalexin, is known to exert numerous beneficial effects in the organism. Isolation of resveratrol from plants, however, has been proved being difficult. Importantly, the bioavailability in the body is poor therefore capability is reduced and not enough resveratrol reaches the target organ. In this study we generated different methoxylated resveratrol analogues using Wittig reaction. trans stilbene obtained was 0.08 g and the cis one was 0.01 g. Additionally with the Horner-Witting method a yield of 0.15 g trans stilbene was obtained. By substituting the hydroxyl group with methoxy group at different positions on the aromatic rings, we could increase the efficacy and bioavailability of the trans form of resveratrol.
Keywords: Cancer; Diabetes; Horner Wittig Reaction; Resveratrol; Stilbene; Wittig Reaction
Abstract| Introduction| Materials and Method| Results and Discussion| Conclusion| Acknowledgement| References|