Bucherer carbazole synthesis
Bucherer carbazole synthesis | |
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Named after | Hans Theodor Bucherer |
Reaction type | Ring forming reaction |
The Bucherer carbazole synthesis is a chemical reaction used to synthesize carbazoles from naphthols and aryl hydrazines using sodium bisulfite. The reaction is named after Hans Theodor Bucherer.
See also
- Borsche-Drechsel cyclization
- Bucherer reaction
References
- Bucherer, Hans Th.; Seyde, Franz (1908). "Über die Einwirkung schwefligsaurer Salze auf aromatische Amino- und Hydroxylverbindungen". J. Prakt. Chem. (in German). 77 (2): 403–413. doi:10.1002/prac.19080770133.
- Drake, Nathan L. (1942). "The Bucherer Reaction". In Adams, Roger (ed.). Organic Reactions. Vol. 1. pp. 63–90. doi:10.1002/0471264180.or001.05. ISBN 9780471264187.
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Topics in organic reactions
- Addition reaction
- Elimination reaction
- Polymerization
- Reagents
- Rearrangement reaction
- Redox reaction
- Regioselectivity
- Stereoselectivity
- Stereospecificity
- Substitution reaction
- A value
- Alpha effect
- Annulene
- Anomeric effect
- Antiaromaticity
- Aromatic ring current
- Aromaticity
- Baird's rule
- Baker–Nathan effect
- Baldwin's rules
- Bema Hapothle
- Beta-silicon effect
- Bicycloaromaticity
- Bredt's rule
- Bürgi–Dunitz angle
- Catalytic resonance theory
- Charge remote fragmentation
- Charge-transfer complex
- Clar's rule
- Conformational isomerism
- Conjugated system
- Conrotatory and disrotatory
- Curtin–Hammett principle
- Dynamic binding (chemistry)
- Edwards equation
- Effective molarity
- Electromeric effect
- Electron-rich
- Electron-withdrawing group
- Electronic effect
- Electrophile
- Evelyn effect
- Flippin–Lodge angle
- Free-energy relationship
- Grunwald–Winstein equation
- Hammett acidity function
- Hammett equation
- George S. Hammond
- Hammond's postulate
- Homoaromaticity
- Hückel's rule
- Hyperconjugation
- Inductive effect
- Kinetic isotope effect
- LFER solvent coefficients (data page)
- Marcus theory
- Markovnikov's rule
- Möbius aromaticity
- Möbius–Hückel concept
- More O'Ferrall–Jencks plot
- Negative hyperconjugation
- Neighbouring group participation
- 2-Norbornyl cation
- Nucleophile
- Kennedy J. P. Orton
- Passive binding
- Phosphaethynolate
- Polar effect
- Polyfluorene
- Ring strain
- Σ-aromaticity
- Spherical aromaticity
- Spiroaromaticity
- Steric effects
- Superaromaticity
- Swain–Lupton equation
- Taft equation
- Thorpe–Ingold effect
- Vinylogy
- Walsh diagram
- Woodward–Hoffmann rules
- Woodward's rules
- Y-aromaticity
- Yukawa–Tsuno equation
- Zaitsev's rule
- Σ-bishomoaromaticity