| 词条 | Hinsberg oxindole synthesis |
| 释义 |
The Hinsberg oxindole synthesis is a method of preparing oxindoles from the bisulfite adducts of glyoxal.[1][2] It is named after its inventor Oscar Hinsberg.[3][4][5] See also
References1. ^{{cite book|author=Elderfield, R.C. |title= Heterocyclic Compounds |volume=3|year=1952|place= New York|page=139}} 2. ^{{cite journal|last1=Murthy|first1=Sabbavarapu Narayana|last2=Madhav|first2=Bandaru|last3=Nageswar|first3=Yadavalli Venkata Durga|title=Revisiting the Hinsberg Reaction: Facile and Expeditious Synthesis of 3-Substituted Quinoxalin-2(1H)-ones under Catalyst-Free Conditions in Water|journal=Helvetica Chimica Acta|date=15 June 2010|volume=93|issue=6|pages=1216–1220|doi=10.1002/hlca.200900358}} 3. ^{{cite journal|author=Hinsberg, O. |journal=Ber. Dtsch. Chem. Ges.|year=1888|volume=21|page= 110|doi=10.1002/cber.18880210122|title=Ueber die Einwirkung der Natriumbisulfitverbindung des Glyoxals auf aromatische Monamine}} 4. ^{{cite journal|last1=Hinsberg|first1=O.|last2=Simeoff|first2=A.|title=Synthese von Naphtindolderivaten|journal=Berichte der deutschen chemischen Gesellschaft|date=January 1898|volume=31|issue=1|pages=250–254|doi=10.1002/cber.18980310150}} 5. ^{{cite journal|author=Hinsberg, O. |journal=Ber. Dtsch. Chem. Ges.|year=1908|volume=41|page= 1367|doi=10.1002/cber.190804101252|title=Über Glykokoll und Indol-derivate}} 1 : Name reactions |
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