Journal
RSC ADVANCES
Volume 12, Issue 13, Pages 8188-8192Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ra00441k
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Funding
- Masaryk University Brno [MUNI/A/1682/2020]
- Czech Science Foundation [GF21-38204L]
- SustES-Adaptation strategies for sustainable ecosystem services and food security under adverse environmental conditions [CZ.02.1.01/0.0/0.0/16_019/0000797]
- Ministry of Education, Youth and Sports of CR within the CzeCOS program [LM2018123]
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An efficient and versatile synthesis method for the naturally occurring C-prenylated stilbenoid methyl ethers and their synthetic analogues is presented. The synthesis involves a six-step convergent process which includes an optimized C-prenylation method. Additionally, six new dihydro-benzopyranyl derivatives were obtained and isolated during the demethylation process.
An efficient and versatile synthesis of the naturally occurring C-prenylated stilbenoid methyl ethers and their synthetic analogues is presented. The synthesis represents a six step convergent process including an optimised C-prenylation method. Furthermore, during the demethylation process, six new dihydro-benzopyranyl derivatives were obtained and isolated.
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