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Rauniticine-allo-oxindole B methanol monosolvate.

ABSTRACT: The title penta-cyclic oxindole alkadoid, isolated from Uncaria longiflora, crystallizes as a methanol solvate, C(20)H(22)N(2)O(4)·CH(4)O. The five-membered ring comprising the indole fused ring is nearly planar [maximum atomic deviation = 0.031?(2)?Å], whereas the five-membered ring having alphatic C atoms adopts an envelope shape (with the tertiary N atom representing the flap). The six-membered ring that shares an N atom with the envelope-shaped ring adopts a chair shape; the six-membered ring having an O atom is sofa-shaped. The carb-oxy-lic acid group acts as a hydrogen-bond donor to a methanol mol-ecule; this, in turn, acts as a hydrogen-bond donor to the double-bond carboxyl O atom of an adjacent mol-ecule, generating a chain. Adjacent chains are linked by N-H?O hydrogen bonds, forming a layer motif.

SUBMITTER: Salim F

PROVIDER: S-EPMC3120594 | biostudies-literature | 2011 Jun

REPOSITORIES: biostudies-literature

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Rauniticine-allo-oxindole B methanol monosolvate.

Salim Fatimah F Ahmad Rohaya R Ismail Nor Hadiani NH Hazni Hazrina H Ng Seik Weng SW

Acta crystallographica. Section E, Structure reports online 20110507 Pt 6

The title penta-cyclic oxindole alkadoid, isolated from Uncaria longiflora, crystallizes as a methanol solvate, C(20)H(22)N(2)O(4)·CH(4)O. The five-membered ring comprising the indole fused ring is nearly planar [maximum atomic deviation = 0.031 (2) Å], whereas the five-membered ring having alphatic C atoms adopts an envelope shape (with the tertiary N atom representing the flap). The six-membered ring that shares an N atom with the envelope-shaped ring adopts a chair shape; the six-membered rin ...[more]

PMID: 21754740

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