Unknown

Dataset Information

0

10?-Hy-droxy-13-{[4-(4-meth-oxy-phen-yl)piperazin-1-yl]meth-yl}-4,9-dimethyl-3,8,15-trioxatetra-cyclo-[10.3.0.0.0]penta-decan-14-one.


ABSTRACT: The title compound, C(26)H(36)N(2)O(6), was synthesized from 9?-hy-droxy-parthenolide (9?-hy-droxy-4,8-dimethyl-12-methylen-3,14-dioxa-tricyclo-[9.3.0.0(2,4)]tetra-dec-7-en-13-one), which was isolated from the chloro-form extract of the aerial parts of Anvillea radiata. The mol-ecule is built up from fused five- and ten-membered rings with two additional ep-oxy ring systems and a meth-oxy-phenyl-piperazine group as a substituent. The ten-membered ring adopts an approximate chair-chair conformation, while the piperazine ring displays a chair conformation and the five-membered ring shows an envelope conformation with the C atom closest to the hy-droxy group forming the flap. The mol-ecular conformation is determined by an O-H?N hydrogen bond between the hy-droxy group and a piperazine N atom. The crystal structure is built up by weak C-H?O inter-actions.

SUBMITTER: Moumou M 

PROVIDER: S-EPMC3295488 | biostudies-other | 2012 Mar

REPOSITORIES: biostudies-other

altmetric image

Publications

10α-Hy-droxy-13-{[4-(4-meth-oxy-phen-yl)piperazin-1-yl]meth-yl}-4,9-dimethyl-3,8,15-trioxatetra-cyclo-[10.3.0.0.0]penta-decan-14-one.

Moumou Mohamed M   Benharref Ahmed A   Daran Jean Claude JC   Outouch Rachid R   Berraho Moha M  

Acta crystallographica. Section E, Structure reports online 20120217 Pt 3


The title compound, C(26)H(36)N(2)O(6), was synthesized from 9α-hy-droxy-parthenolide (9α-hy-droxy-4,8-dimethyl-12-methylen-3,14-dioxa-tricyclo-[9.3.0.0(2,4)]tetra-dec-7-en-13-one), which was isolated from the chloro-form extract of the aerial parts of Anvillea radiata. The mol-ecule is built up from fused five- and ten-membered rings with two additional ep-oxy ring systems and a meth-oxy-phenyl-piperazine group as a substituent. The ten-membered ring adopts an approximate chair-chair conformati  ...[more]

Similar Datasets

| S-EPMC3344453 | biostudies-literature
| S-EPMC3247384 | biostudies-literature
| S-EPMC3151905 | biostudies-other
| S-EPMC3254508 | biostudies-literature
| S-EPMC3344091 | biostudies-literature
| S-EPMC4011210 | biostudies-literature
| S-EPMC3247403 | biostudies-literature
| S-EPMC3998562 | biostudies-literature
| S-EPMC3297315 | biostudies-literature
| S-EPMC3394072 | biostudies-literature