benzofurans has been researched along with serotobenine* in 3 studies
1 review(s) available for benzofurans and serotobenine
| Article | Year |
|---|---|
Synthetic approaches to natural products containing 2,3-dihydrobenzofuran skeleton.
Covering: 2000 to 2018 Natural products containing the 2,3-dihydrobenzofuran (2,3-DHB) skeleton have been the focus of a substantial number of synthetic studies since 2000. Herein, we review the total syntheses of decursivine, serotobenine, lithospermic acid, linderol A, bisabosqual A, pterocarpans, conocarpan, heliannuols, and some resveratrol oligomers, with emphasis on the synthetic strategies employed. Topics: Benzofurans; Biological Products; Depsides; Heterocyclic Compounds, 4 or More Rings; Indole Alkaloids; Indoles; Molecular Structure | 2019 |
2 other study(ies) available for benzofurans and serotobenine
| Article | Year |
|---|---|
Palladium-catalyzed synthesis of benzofurans via C-H activation/oxidation tandem reaction and its application to the synthesis of decursivine and serotobenine.
A new palladium-catalyzed method for the synthesis of benzofurans by reaction of 2-hydroxystyrenes and iodobenzenes via a C-H activation/oxidation tandem reaction has been unprecedentedly discovered. By using this strategy, the overall synthetic efficiency of the synthesis of decursivine and its analogues was indeed improved. Preliminary mechanistic studies shed light into the possible mechanisms. Topics: Benzofurans; Carbon; Catalysis; Hydrogen; Indole Alkaloids; Indoles; Oxidation-Reduction; Palladium | 2014 |
Total synthesis of (-)-serotobenine.
The efficient total synthesis of (-)-serotobenine (1) has been achieved by constructing an optically active dihydrobenzofuran ring via a rhodium carbenoid mediated intramolecular C-H insertion reaction, which was developed by our group. Then the possibility of racemization of 1 was investigated using optically active synthetic 1. Topics: Benzofurans; Indoles; Isomerism; Molecular Structure | 2008 |