Unknown

Dataset Information

0

(4aS,10aS)-7-Hydr-oxy-8-isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octa-hydro-phenanthrene: a new diterpenoid compound.


ABSTRACT: The new title diterpenoid compound, C(20)H(30)O, is a natural product isolated from Tetra-clinis articulata wood via chloro-form extraction. The asymmetric unit contains four mol-ecules with the same S,S configuration, deduced from the chemical synthesis. Indeed, an overlay analysis, calculated using structure-matching software, shows that the four mol-ecules can be superimposed. The central ring has a half-chair conformation, whereas the saturated ring displays a chair conformation.

SUBMITTER: Zeroual A 

PROVIDER: S-EPMC2960765 | biostudies-literature | 2008 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

(4aS,10aS)-7-Hydr-oxy-8-isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octa-hydro-phenanthrene: a new diterpenoid compound.

Zeroual Abdellah A   Mazoir Noureddine N   Daran Jean-Claude JC   Akssira Mohamed M   Benharref Ahmed A  

Acta crystallographica. Section E, Structure reports online 20080220 Pt 3


The new title diterpenoid compound, C(20)H(30)O, is a natural product isolated from Tetra-clinis articulata wood via chloro-form extraction. The asymmetric unit contains four mol-ecules with the same S,S configuration, deduced from the chemical synthesis. Indeed, an overlay analysis, calculated using structure-matching software, shows that the four mol-ecules can be superimposed. The central ring has a half-chair conformation, whereas the saturated ring displays a chair conformation. ...[more]

Similar Datasets

| S-EPMC3515197 | biostudies-literature
| S-EPMC2977794 | biostudies-literature
| S-EPMC4647402 | biostudies-literature
| S-EPMC2969610 | biostudies-literature
| S-EPMC2977793 | biostudies-literature
| S-EPMC3011422 | biostudies-other
| S-EPMC2960539 | biostudies-literature
| S-EPMC3238859 | biostudies-other
| S-EPMC2960938 | biostudies-literature
| S-EPMC2961293 | biostudies-other