Cover Picture: Biology-Oriented Synthesis of Stereochemically Diverse Natural-Product-Derived Compound Collections by Iterative Allylations on a Solid Support (Chem. Eur. J. 12/2007)
α,β‐Unsaturated δ‐lactones with multiply oxygenated side chains are a substructure found in a group of natural products with a broad range of biological activity. In their Full Paper on page 3305 ff., H. Waldmann et al. describe the parallel synthesis of all eight diastereomers of cryptocarya diacet...
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| Veröffentlicht in: | Chemistry : a European journal 2007-04, Vol.13 (12), p.3277-3277 |
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| container_end_page | 3277 |
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| container_issue | 12 |
| container_start_page | 3277 |
| container_title | Chemistry : a European journal |
| container_volume | 13 |
| creator | Umarye, Jayant D. Leßmann, Torben García, Ana B. Mamane, Victor Sommer, Stefan Waldmann, Herbert |
| description | α,β‐Unsaturated δ‐lactones
with multiply oxygenated side chains are a substructure found in a group of natural products with a broad range of biological activity. In their Full Paper on page 3305 ff., H. Waldmann et al. describe the parallel synthesis of all eight diastereomers of cryptocarya diacetate by asymmetric allylation reactions on a solid support with chiral allylboranes. |
| doi_str_mv | 10.1002/chem.200790036 |
| format | Article |
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| ispartof | Chemistry : a European journal, 2007-04, Vol.13 (12), p.3277-3277 |
| issn | 0947-6539 1521-3765 |
| language | eng |
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| source | Wiley Online Library All Journals |
| subjects | 3-polyols asymmetric synthesis natural products solid-phase synthesis |
| title | Cover Picture: Biology-Oriented Synthesis of Stereochemically Diverse Natural-Product-Derived Compound Collections by Iterative Allylations on a Solid Support (Chem. Eur. J. 12/2007) |
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