Abstract
The C7H11NO2 compound, an intermediate in a synthetic approach to the pyrrolizidine alkaloid loline was discussed. The compound has a brendane skeleton with a 91.8(2)° bond angle for the bridging carbon bearing the OH group. The x-ray show that the molecule was an analog of brendane. The results show that the molecules of compound form infinite linear chains through hydrogen bonding of the alcohol moiety of one molecule with the amine moiety of the next molecule.
| Language | English (US) |
|---|---|
| Journal | Acta Crystallographica Section E: Structure Reports Online |
| Volume | 59 |
| Issue number | 9 |
| DOIs | |
| State | Published - Sep 2003 |
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ASJC Scopus subject areas
- Condensed Matter Physics
- Structural Biology
Cite this
(1a,6a,7a,7aβ)-2,3,5,6,7,7a-Hexahydro-1,6-epoxy-1H-pyrrolizin-7-ol. / Glass, Richard S; Deardorff, Donald R.; Stessman, Nhu Y T; Carducci, Michael D.
In: Acta Crystallographica Section E: Structure Reports Online, Vol. 59, No. 9, 09.2003.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - (1a,6a,7a,7aβ)-2,3,5,6,7,7a-Hexahydro-1,6-epoxy-1H-pyrrolizin-7-ol
AU - Glass, Richard S
AU - Deardorff, Donald R.
AU - Stessman, Nhu Y T
AU - Carducci, Michael D.
PY - 2003/9
Y1 - 2003/9
N2 - The C7H11NO2 compound, an intermediate in a synthetic approach to the pyrrolizidine alkaloid loline was discussed. The compound has a brendane skeleton with a 91.8(2)° bond angle for the bridging carbon bearing the OH group. The x-ray show that the molecule was an analog of brendane. The results show that the molecules of compound form infinite linear chains through hydrogen bonding of the alcohol moiety of one molecule with the amine moiety of the next molecule.
AB - The C7H11NO2 compound, an intermediate in a synthetic approach to the pyrrolizidine alkaloid loline was discussed. The compound has a brendane skeleton with a 91.8(2)° bond angle for the bridging carbon bearing the OH group. The x-ray show that the molecule was an analog of brendane. The results show that the molecules of compound form infinite linear chains through hydrogen bonding of the alcohol moiety of one molecule with the amine moiety of the next molecule.
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UR - http://www.scopus.com/inward/citedby.url?scp=18444374382&partnerID=8YFLogxK
U2 - 10.1107/S1600536803016970
DO - 10.1107/S1600536803016970
M3 - Article
VL - 59
JO - Acta Crystallographica Section E: Structure Reports Online
T2 - Acta Crystallographica Section E: Structure Reports Online
JF - Acta Crystallographica Section E: Structure Reports Online
SN - 1600-5368
IS - 9
ER -