Unknown

Dataset Information

0

(1S,3S,8R,9S,11R)-10,10-Di-chloro-3,7,7,11-tetra-methyl-tetra-cyclo[6.5.0.0(1,3).0(9,11)]trideca-ne.


ABSTRACT: The title compound, C17H26Cl2, was synthesized from ?-himachalene (3,5,5,9-tetra-methyl-2,4a,5,6,7,8-hexa-hydro-1H-benzo-cyclo-heptene), which was isolated from the essential oil of the Atlas cedar (Cedrus Atlantica). The asymmetric unit contains two independent mol-ecules with similar conformations. Each mol-ecule is built up from fused six- and seven-membered rings and two three-membered rings from the reaction of ?-himachalene with di-chloro-carbene. In both mol-ecules, the six-membered ring has a half-chair conformation, whereas the seven-membered ring displays a boat conformation. The absolute configuration was established from anomalous dispersion effects.

SUBMITTER: Benharref A 

PROVIDER: S-EPMC3685081 | biostudies-literature | 2013 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications

(1S,3S,8R,9S,11R)-10,10-Di-chloro-3,7,7,11-tetra-methyl-tetra-cyclo[6.5.0.0(1,3).0(9,11)]trideca-ne.

Benharref Ahmed A   Ourhriss Najia N   El Ammari Lahcen L   Saadi Mohamed M   Berraho Moha M  

Acta crystallographica. Section E, Structure reports online 20130522 Pt 6


The title compound, C17H26Cl2, was synthesized from β-himachalene (3,5,5,9-tetra-methyl-2,4a,5,6,7,8-hexa-hydro-1H-benzo-cyclo-heptene), which was isolated from the essential oil of the Atlas cedar (Cedrus Atlantica). The asymmetric unit contains two independent mol-ecules with similar conformations. Each mol-ecule is built up from fused six- and seven-membered rings and two three-membered rings from the reaction of β-himachalene with di-chloro-carbene. In both mol-ecules, the six-membered ring  ...[more]

Similar Datasets

| S-EPMC3793758 | biostudies-literature
| S-EPMC3648256 | biostudies-literature
| S-EPMC3648270 | biostudies-literature
| S-EPMC3569802 | biostudies-other
| S-EPMC3629633 | biostudies-literature
| S-EPMC3414157 | biostudies-literature
| S-EPMC3998592 | biostudies-literature
| S-EPMC3793829 | biostudies-other
| S-EPMC3793796 | biostudies-other
| S-EPMC4719952 | biostudies-literature