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Bonvalotidine A acetone solvate from Delphinium bonvalotii Franch.


ABSTRACT:

The title compound (systematic name

5,6?-dihy-droxy-1?,14?,16?-trimeth-oxy-4-methyl-7?,8-methyl-enedi-oxy-20-ethyl-aconitan-6-yl acetate acetone monosolvate), C(27)H(41)NO(8)·C(3)H(6)O, was isolated from Delphinium bonvalotii Franch, and is a typical C(19)-diterpenoid alkaloid. The mol-ecule has a lycoctonine carbon skeleton with four six-membered rings and three five-membered rings. Three six-membered rings adopt the chair conformations while the fourth adopts a boat conformation, while the five-membered rings have the envelope conformations. The solvent mol-ecule links with the organic mol-ecule via a classical O-H?O hydrogen bond. Weak C-H?O hydrogen bonding is present in the structure. An intra-molecular O-H?O hydrogen bond also occurs.

SUBMITTER: Li SH 

PROVIDER: S-EPMC3011611 | biostudies-literature | 2010 Nov

REPOSITORIES: biostudies-literature

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Bonvalotidine A acetone solvate from Delphinium bonvalotii Franch.

Li Shu-Hua SH   Chen Feng-Zheng FZ  

Acta crystallographica. Section E, Structure reports online 20101127 Pt 12


<h4>The title compound (systematic name</h4>5,6β-dihy-droxy-1α,14α,16β-trimeth-oxy-4-methyl-7β,8-methyl-enedi-oxy-20-ethyl-aconitan-6-yl acetate acetone monosolvate), C(27)H(41)NO(8)·C(3)H(6)O, was isolated from Delphinium bonvalotii Franch, and is a typical C(19)-diterpenoid alkaloid. The mol-ecule has a lycoctonine carbon skeleton with four six-membered rings and three five-membered rings. Three six-membered rings adopt the chair conformations while the fourth adopts a boat conformation, while  ...[more]

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