Total Synthesis of Marine Oxylipins Solandelactones A-H
The Solandelactones A–H have been synthesized via a short convergent approach utilizing common building blocks. Based on the diastereoselectivity of the crucial final addition step and on the comparison of prominent NMR data, a structural revision was necessary.
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| Veröffentlicht in: | Advanced synthesis & catalysis 2008-06, Vol.350 (9), p.1407-1412 |
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| container_end_page | 1412 |
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| container_issue | 9 |
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| container_title | Advanced synthesis & catalysis |
| container_volume | 350 |
| creator | Pietruszka, Jörg Rieche, Anja C. M. |
| description | The Solandelactones A–H have been synthesized via a short convergent approach utilizing common building blocks. Based on the diastereoselectivity of the crucial final addition step and on the comparison of prominent NMR data, a structural revision was necessary. |
| doi_str_mv | 10.1002/adsc.200800198 |
| format | Article |
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| ispartof | Advanced synthesis & catalysis, 2008-06, Vol.350 (9), p.1407-1412 |
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| language | eng |
| recordid | cdi_proquest_miscellaneous_33522082 |
| source | Wiley-Blackwell Journals |
| subjects | asymmetric synthesis cyclopropanes natural products structure elucidation total synthesis |
| title | Total Synthesis of Marine Oxylipins Solandelactones A-H |
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