ChemInform Abstract: Convergent Syntheses of 3,6-Dihydroxydec-4-enolides
A Nozaki—Hiyama—Kishi cyclization which creates the (6R) stereocenter in the ring system is the key step in the synthesis of the novel dihydroxy decanolide (Vb) and the known diastereomer (IXb), a constituent of Cordyceps militaris.
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| Veröffentlicht in: | ChemInform 2012-12, Vol.43 (50), p.no-no |
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| creator | Killen, Jonathan C. Axford, Lorraine C. Newberry, Sarah E. Simpson, Thomas J. Willis, Christine L. |
| description | A Nozaki—Hiyama—Kishi cyclization which creates the (6R) stereocenter in the ring system is the key step in the synthesis of the novel dihydroxy decanolide (Vb) and the known diastereomer (IXb), a constituent of Cordyceps militaris. |
| doi_str_mv | 10.1002/chin.201250205 |
| format | Article |
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| language | eng |
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| subjects | antibiotics medicinal chemistry pharmacology pharmacology, medicinal chemistry, vaccines, serums serums vaccines |
| title | ChemInform Abstract: Convergent Syntheses of 3,6-Dihydroxydec-4-enolides |
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