| Reference Type | Journal (article/letter/editorial) |
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| Title | Conessine isolated from Holarrhena floribunda |
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| Journal | Acta Crystallographica Section E Structure Reports Online |
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| Authors | Lannang, Alain Meli | Author |
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| Anjum, Shazia | Author |
| Tangmouo, Jean Gustave | Author |
| Krohn, Karsten | Author |
| Choudhary, M. Iqbal | Author |
| Year | 2007 (November 1) | Volume | 63 |
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| Issue | 11 |
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| Publisher | International Union of Crystallography (IUCr) |
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| DOI | doi:10.1107/s1600536807051215Search in ResearchGate |
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| Generate Citation Formats |
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| Mindat Ref. ID | 467503 | Long-form Identifier | mindat:1:5:467503:1 |
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| GUID | 0 |
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| Full Reference | Lannang, Alain Meli, Anjum, Shazia, Tangmouo, Jean Gustave, Krohn, Karsten, Choudhary, M. Iqbal (2007) Conessine isolated from Holarrhena floribunda. Acta Crystallographica Section E Structure Reports Online, 63 (11) doi:10.1107/s1600536807051215 |
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| Plain Text | Lannang, Alain Meli, Anjum, Shazia, Tangmouo, Jean Gustave, Krohn, Karsten, Choudhary, M. Iqbal (2007) Conessine isolated from Holarrhena floribunda. Acta Crystallographica Section E Structure Reports Online, 63 (11) doi:10.1107/s1600536807051215 |
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| In | (2007, November) Acta Crystallographica Section E Structure Reports Online Vol. 63 (11) International Union of Crystallography (IUCr) |
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| Abstract/Notes | The title compound, C24H40N2, has been isolated from Holarrhena floribunda G. Don. (Apocynaceae). The compound has a pentacyclic steroidal nucleus; the ring junctions share the same stereochemistry reported for this class of compounds. Of the three six-membered rings, rings A and C adopt a chair-like and ring B forms a half-chair-like conformation. The cyclopentane ring D shows a half-chair conformation and the methylpyrrolidine ring E adopts an envelope conformation. The dimethylamino substituent in ring A is equatorially oriented. |
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