Chemistry:Hinsberg oxindole synthesis
From HandWiki
Revision as of 11:39, 30 June 2021 by imported>BotanyGa (simplify)
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
- Friedel-Crafts alkylation
- Stolle synthesis
- Hinsberg reaction
References
- ↑ Elderfield, R.C. (1952). Heterocyclic Compounds. 3. New York. p. 139.
- ↑ 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. https://zenodo.org/record/1425525.
- ↑ Hinsberg, O.; Simeoff, A. (January 1898). "Synthese von Naphtindolderivaten". Berichte der Deutschen Chemischen Gesellschaft 31 (1): 250–254. doi:10.1002/cber.18980310150. https://zenodo.org/record/1425902.
- ↑ Hinsberg, O. (1908). "Über Glykokoll und Indol-derivate". Ber. Dtsch. Chem. Ges. 41: 1367. doi:10.1002/cber.190804101252. https://zenodo.org/record/1426277.
 |  |
