Secohellebrigeninamide.
Acta Crystallogr Sect E Struct Rep Online
; 68(Pt 3): o682, 2012 Mar 01.
Article
em En
| MEDLINE
| ID: mdl-22412577
The title compound, C(26)H(37)NO(5), was the reaction product of hellebrigenin with N,N-dimethyl-formamide. It consists of three cyclo-hexane rings (A, B and C), one five-membered ring (D) and one dihydro-pyran ring (E). The stereochemistry of the ring junctions is is A/B cis, B/C trans, C/D cis and C/E trans. The cyclo-hexane rings A, B and C have chair conformations. Both the five-membered ring D and the dihydro-pyran ring adopt an envelope conformation. Two orientations are found for the aldehyde group with occupancies of 0.608â
(10) and 0.392â
(10). In the crystal, short O-Hâ¯O hydrogen bonds and short C-Hâ¯O contacts involving the hy-droxy group, terminal methyl group and carbonyl group link the mol-ecules into a three-dimensional network.
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MEDLINE
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En
Ano de publicação:
2012
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Article