Regioselective Biomimetic Synthesis of Dimeric Oxyresveratrol Derivatives

Lu Ran; Hongpeng Li; Ge Chao; Xiaodong Kang; Tian Lei; Wenling Li

doi:10.1055/s-0040-1707257

Synlett, Inhaltsverzeichnis

Synlett 2020; 31(18): 1809-1812
DOI: 10.1055/s-0040-1707257

letter

Regioselective Biomimetic Synthesis of Dimeric Oxyresveratrol Derivatives

Authors

Lu Ran
Hongpeng Li
Ge Chao
Xiaodong Kang
Tian Lei
Wenling Li∗

School of Chemical and Biological Engineering, Lanzhou Jiaotong University, Lanzhou 730070, P. R. of China

Abstract

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Abstract

Oxyresveratrol and its methylated derivative as coupling precursors were efficiently prepared in four steps, with Wittig reactions and subsequent isomerization reactions as the key steps. The coupling reactions of oxyresveratrol under various oxidative conditions gave a complex and inseparable mixture of coupling products. The oxidative dimerizations of methylated oxyresveratrols catalyzed by horseradish peroxidase–H₂O₂ or FeCl₃·6H₂O in an acetone system predominantly produced the 8–5-coupled and 8–10-coupled dihydrobenzofuran-type dimers, respectively. This regioselective biomimetic strategy might be useful in synthesizing other dimeric oxyresveratrol derivatives.

Key words

oxyresveratrol - biomimetic synthesis - oligostilbenes - oxidative coupling - dimerization - regioselectivity

Volltext

Referenzen

References and Notes

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14 5-[(E)-2-(4-Hydroxy-2-methoxyphenyl)ethenyl]benzene-1,3-diol [(E)-15] Pale-yellow oil; yield: 1.77 g (91%). ¹H NMR (500 MHz, acetone-d ₆): δ = 3.85 (s, 3 H), 6.24 (t, J = 2.0 Hz, 1 H), 6.46 (dd, J = 8.5, 2.0 Hz, 1 H), 6.49 (d, J = 2.0 Hz, 1 H), 6.52 (d, J = 2.0 Hz, 2 H), 6.88 (d, J = 16.5 Hz, 1 H), 7.30 (d, J = 16.5 Hz, 1 H), 7.45 (d, J = 8.5 Hz, 1 H), 8.16 (br s, 2 H), 8.51 (br s, 1 H). ¹³C NMR (125 MHz, acetone-d ₆): δ = 55.8, 99.8, 99.9, 102.4, 105.5 (2 C), 108.5, 118.7, 123.9, 126.8, 127.9, 141.5, 159.2, 159.5, 159.6. HRMS (ESI): m/z [M –H]⁺ calcd for C₁₅H₁₃O₄: 257.08193; found: 257.08191.
15 5-{(E)-2-[3-(3,5-Dihydroxyphenyl)-2-(4-hydroxy-2-methoxyphenyl)-6-methoxy-2,3-dihydro-1-benzofuran-5-yl]ethenyl}benzene-1,3-diol (16) Yellowish amorphous powder; yield: 31 mg (62%). ¹H NMR (500 MHz, acetone-d ₆): δ = 3.77 (s, 3 H), 3.94 (s, 3 H), 4.36 (d, J = 5.0 Hz, 1 H), 5.73 (d, J = 5.0 Hz, 1 H), 6.21 (d, J = 2.0 Hz, 2 H), 6.23 (t, J = 2.0 Hz, 1 H), 6.24 (t, J = 2.0 Hz, 1 H), 6.40 (dd, J = 8.5, 2.0 Hz, 1 H), 6.50 (d, J = 2.0 Hz, 2 H), 6.52 (d, J = 2.0 Hz, 1 H), 6.64 (d, J = 2.0 Hz, 1 H), 6.84 (d, J = 16.5 Hz, 1 H), 7.12 (d, J = 8.5 Hz, 1 H), 7.32 (d, J = 2.0 Hz, 1 H), 7.35 (d, J = 16.5 Hz, 1 H), 8.15 (br s, 2 H), 8.16 (br s, 2 H), 8.46 (br s, 1 H). ¹³C NMR (125 MHz, acetone-d ₆): δ = 55.7, 56.2, 89.8, 94.3, 100.0, 102.0, 102.5, 105.5, 105.6 (2 C), 107.0, 107.1 (2 C), 107.6, 119.8, 121.2, 122.9 (2 C), 123.4, 123.9, 126.8, 128.1, 141.4, 147.2, 159.0, 159.1, 159.5, 159.6 (2 C), 162.2. HRMS (ESI): m/z [M – H]⁺ calcd for C₃₀H₂₅O₈: 513.15549; found: 513.15547.
16 5-{6-Hydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-[(E)-2-(3-hydroxy-5-methoxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl}benzene-1,3-diol (18) Yellowish amorphous powder; yield: 15 mg (45%). ¹H NMR (500 MHz, acetone-d ₆): δ = 3.76 (s, 3 H), 3.83 (s, 3 H), 4.36 (d, J = 5.0 Hz, 1 H), 5.67 (d, J = 5.0 Hz, 1 H), 6.20 (dd, J = 8.5, 2.0 Hz, 1 H), 6.26 (d, J = 2.0 Hz, 2 H), 6.34 (dd, J = 8.0, 2.0 Hz, 1 H), 6.36 (d, J = 2.0 Hz, 2 H), 6.41 (d, J = 2.0 Hz, 1 H), 6.51 (d, J = 2.0 Hz, 1 H), 6.68 (d, J = 2.0 Hz, 1 H), 6.76 (d, J = 16.5 Hz, 1 H), 7.05 (d, J = 8.0 Hz, 1 H), 7.15 (d, J = 16.5 Hz, 1 H), 7.16 (d, J = 8.0 Hz, 1 H). ¹³C NMR (125 MHz, acetone-d ₆): δ = 55.6, 55.7, 55.8, 89.1, 99.7, 99.8, 103.9, 107.0, 107.3, 108.3, 118.6, 120.1, 122.3, 123.8, 125.3, 125.6, 127.2, 127.8, 128.1, 128.4, 137.2, 148.1, 151.9, 158.5 (2 C), 159.3 (2 C), 159.5, 162.8 (2 C). HRMS (ESI): m/z [M – H]⁺ calcd for C₃₀H₂₅O₈: 513.15549; found: 513.15546.

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