A thermal 6pi electrocyclization strategy towards taiwaniaquinoids. First enantiospecific synthesis of (-)-taiwaniaquinone G
The first route towards taiwaniaquinoid terpenes bearing an A/B trans-configuration has been developed through a sequence which includes a thermal 6pi electrocyclization.
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| Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2009-02 (5), p.592-594 |
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| container_title | Chemical communications (Cambridge, England) |
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| creator | Alvarez-Manzaneda, Enrique Chahboun, Rachid Cabrera, Eduardo Alvarez, Esteban Haidour, Ali Ramos, Jose Miguel Alvarez-Manzaneda, Ramón Hmamouchi, Mohammed Es-Samti, Hakima |
| description | The first route towards taiwaniaquinoid terpenes bearing an A/B trans-configuration has been developed through a sequence which includes a thermal 6pi electrocyclization. |
| doi_str_mv | 10.1039/b816812a |
| format | Article |
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| identifier | ISSN: 1359-7345 |
| ispartof | Chemical communications (Cambridge, England), 2009-02 (5), p.592-594 |
| issn | 1359-7345 |
| language | eng |
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| source | MEDLINE; Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
| subjects | Cyclization Diterpenes - chemical synthesis Diterpenes - chemistry Electrons Stereoisomerism Temperature |
| title | A thermal 6pi electrocyclization strategy towards taiwaniaquinoids. First enantiospecific synthesis of (-)-taiwaniaquinone G |
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