(1a,6a,7a,7aβ)-2,3,5,6,7,7a-Hexahydro-1,6-epoxy-1H-pyrrolizin-7-ol

Richard S. Glass, Donald R. Deardorff, Nhu Y T Stessman, Michael D. Carducci

Research output: Research - peer-reviewArticle

  • 1 Citations

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.

LanguageEnglish (US)
JournalActa Crystallographica Section E: Structure Reports Online
Volume59
Issue number9
DOIs
StatePublished - Sep 2003

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Pyrrolizidine Alkaloids
Hydrogen Bonding
Skeleton
Amines
Carbon
Alcohols
X-Rays
loline
An-2 compound
molecules
Molecules
alkaloids
musculoskeletal system
amines
alcohols
analogs
carbon
hydrogen
x rays
Bearings (structural)

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: Research - peer-reviewArticle

Glass, Richard S. ; Deardorff, Donald R. ; Stessman, Nhu Y T ; Carducci, Michael D./ (1a,6a,7a,7aβ)-2,3,5,6,7,7a-Hexahydro-1,6-epoxy-1H-pyrrolizin-7-ol. In: Acta Crystallographica Section E: Structure Reports Online. 2003 ; Vol. 59, No. 9.
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