Isoxazoline

From Wikipedia, the free encyclopedia
Isoxazoline
2-isoxazoline.svg
2-isoxazoline
3-isoxazoline.svg
3-isoxazoline
4-isoxazoline.svg
4-isoxazoline
Names
Systematic IUPAC name
Respective to images:
4,5-Dihydroisoxazole
2,5-Dihydroisoxazole
2,3-Dihydroisoxazole
Other names
Respective to images:
Δ2-isoxazoline
Δ3-isoxazoline
Δ4-isoxazoline
Identifiers
3D model (JSmol)
ChEBI
  • 2-isoxazoline: InChI=1S/C3H5NO/c1-2-4-5-3-1/h2H,1,3H2
    Key: WEQPBCSPRXFQQS-UHFFFAOYSA-N
  • 2-isoxazoline: C1CON=C1
  • 3-isoxazoline: C1CONC=1
  • 4-isoxazoline: C1=CONC1
Properties
C3H5NO
Molar mass 71.079 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Isoxazolines are a class of five-membered heterocyclic chemical compounds, containing one atom each of oxygen and nitrogen which are located adjacent to one another. The ring was named in-line with the Hantzsch–Widman nomenclature. They are structural isomers of the more common oxazolines and exist in three different isomers depending on the location of the double bond. The relatively weak N-O bond makes isoxazolines prone to ring-opening and rearrangement reactions.

Compounds containing an isoxazoline ring, sometimes referred to isoxazolyls, have a variety of uses with many being biologically active. A number of naturally occurring isoxazolines with possible anti-cancer activity are produced by marine sponges.[1] Perhaps the most commonly encountered products containing isoxazolines are some veterinary medicines used to prevent flea infestations in dogs e.g. Fluralaner, Afoxolaner and Sarolaner.

Synthesis[]

2-Isoxazolines are generally produced by the 1,3-dipolar cycloaddition of nitrile oxides with alkenes.[2] This has been applied in a diastereoselective manner in the synthesis of epothilones.[3]

Use of directed cycloaddition in Epothilones synthesis.tif

3-isoxazolines are prepared from 2-isoxazolines via their N-methylation to form 2-isoxazolinium salts, followed by nucleophilic attack and deprotonation.[4]

4-Isoxazolines are most commonly produced by (3+2) cycloaddition between a nitrone and an alkyne.[5] This can be considered an extension of the more common nitrone-olefin (3+2) cycloaddition used for creating isoxazolidines.

500pxg

See also[]

References[]

  1. ^ Kaur, Kamalneet; Kumar, Vinod; Sharma, Anil Kumar; Gupta, Girish Kumar (April 2014). "Isoxazoline containing natural products as anticancer agents: A review". European Journal of Medicinal Chemistry. 77: 121–133. doi:10.1016/j.ejmech.2014.02.063. PMID 24631731.
  2. ^ Erik Larsen, Karl; Torssell, Kurt B.G. (January 1984). "An improved procedure for the preparation of 2-isoxazolines". Tetrahedron. 40 (15): 2985–2988. doi:10.1016/S0040-4020(01)91313-4.
  3. ^ Bode, Jeffrey; Carreira, Erick (2011). "Stereoselective Syntheses of Epothilones A and B via Directed Nitrile Oxide Cycloaddition". Journal of the American Chemical Society. 123 (15): 3611–3612. doi:10.1021/ja0155635. PMID 11472140.
  4. ^ Jäger, Volker; Frey, Wolfgang; Bathich, Yaser; Shiva, Sunitha; Ibrahim, Mohammad; Henneböhle, Marco; LeRoy, Pierre-Yves; Imerhasan, Mukhtar (1 July 2010). "2-Isoxazolinium Salts and 3-Isoxazolines: Exploratory Chemistry and Uses for the Synthesis of Branched Amino Polyols and Amino Acids". Zeitschrift für Naturforschung B. 65 (7): 821–832. doi:10.1515/znb-2010-0708. S2CID 12345097.open access
  5. ^ Freeman, Jeremiah P. (June 1983). ".DELTA.4-Isoxazolines (2,3-dihydroisoxazoles)". Chemical Reviews. 83 (3): 241–261. doi:10.1021/cr00055a002.
Retrieved from ""