Pyrrolizidine

Pyrrolizidine is a heterocyclic organic compound that forms the central chemical structure of a variety of alkaloids known collectively as pyrrolizidine alkaloids.[1] It is one of five classes of iminosugars. These are often synthesized from a carbohydrate.[2]

Pyrrolizidine
Names
Preferred IUPAC name
Hexahydro-1H-pyrrolizine
Other names
Hexahydropyrrolizine
1-Azabicyclo[3.3.0]octane
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.117.254
UNII
  • InChI=1S/C7H13N/c1-3-7-4-2-6-8(7)5-1/h7H,1-6H2 checkY
    Key: ADRDEXBBJTUCND-UHFFFAOYSA-N checkY
  • InChI=1/C7H13N/c1-3-7-4-2-6-8(7)5-1/h7H,1-6H2
    Key: ADRDEXBBJTUCND-UHFFFAOYAT
  • N12CCCC1CCC2
Properties
C7H13N
Molar mass 111.18 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references

References
  1. Pyrrolizidine alkaloids at KEGG Archived 2016-03-03 at the Wayback Machine
  2. Lauritsen, Anne; Madsen, Robert (2006-07-19). "Synthesis of naturally occurring iminosugars from D-fructose by the use of a zinc-mediated fragmentation reaction". Organic & Biomolecular Chemistry. 4 (15): 2898–2905. doi:10.1039/B605818C. ISSN 1477-0539. PMID 16855738.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.