The Hinsberg oxindole synthesis is a method of preparing oxindoles from the bisulfite additions of glyoxal.[1][2] It is named after its inventor Oscar Hinsberg.[3][4][5]
See also
References
- ^ Elderfield, R.C. (1952). Heterocyclic Compounds. Vol. 3. New York. p. 139.
{{cite book}}: CS1 maint: location missing publisher (link) - ^ Murthy, Sabbavarapu Narayana; Madhav, Bandaru; Nageswar, Yadavalli Venkata Durga (15 June 2010). "Revisiting the Hinsberg Reaction: Facile and Expeditious Synthesis of 3-Substituted Quinoxalin-2(1H)-ones under Catalyst-Free Conditions in Water". Helvetica Chimica Acta. 93 (6): 1216–1220. doi:10.1002/hlca.200900358.
- ^ Hinsberg, O. (1888). "Ueber die Einwirkung der Natriumbisulfitverbindung des Glyoxals auf aromatische Monamine". Ber. Dtsch. Chem. Ges. 21: 110. doi:10.1002/cber.18880210122.
- ^ Hinsberg, O.; Simeoff, A. (January 1898). "Synthese von Naphtindolderivaten". Berichte der Deutschen Chemischen Gesellschaft. 31 (1): 250–254. doi:10.1002/cber.18980310150.
- ^ Hinsberg, O. (1908). "Über Glykokoll und Indol-derivate". Ber. Dtsch. Chem. Ges. 41: 1367. doi:10.1002/cber.190804101252.
This page was last edited on 24 September 2020, at 10:38