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Indoles
Nitrogen heterocycles
Aromatic compounds
Heterocyclic compounds
Simple aromatic rings

Summary Of: Indole

in the aromatic ring means that indole is not a... Indole can be produced by... The indole structure can be found in many organic compounds like the... since indole was first isolated by treatment of the indigo dye with oleum... Indole chemistry began to develop with the study of the dye... indole to indole using... Certain indole derivatives were important dyestuffs until the end of the 19th century... interest in indole intensified when it became known that the indole nucleus is present in many important... Indole is a major constituent of... Indole and its derivatives can also be synthesized by a variety of methods... is an efficient method of sythesizing indole and substituted indoles... Although the synthesis of indole itself is problematic using the Fischer indole synthesis... of the resulting indole anion can react in two ways... bond of indole is capable of...

Encyclodia Page On: Indole

These Are Links To Other Documents
Chemical structure of indole | IUPAC name | CAS number | RTECS number | SMILES | ChemSpider | Molecular formula | Molar mass | Density | Melting point | Boiling point | Solubility | water | Acidity | DMSO | Basicity | Crystal structure | Molecular shape | Dipole moment | D | benzene | MSDS | R/S statement | Flash point | aromatic
compounds
| benzene | benzofuran | carbazole | carboline | indene | indoline | isatin | methylindole | oxindole | pyrrole | skatole | standard state
(at 25 °C, 100 kPa)
| Infobox references | aromatic | heterocyclic | organic compound | benzene | nitrogen | pyrrole | lone electron pair | base | amine | solid | bacteria | amino acid | tryptophan | feces | odor | scents | perfumes | coal tar | amino acid | tryptophan | protein | alkaloids | pigments | electrophilic substitution | tryptamine | neurotransmitter | serotonin | melatonin | Auxin | IAA | indomethacin | betablocker | pindolol | portmanteau | indigo | oleum | Baeyer's original structure for indole, 1869 | | indigo | isatin | oxindole | 1866 | Adolf von Baeyer | zinc | 1930s | alkaloids | tryptophan | auxins | coal-tar | Leimgruber-Batcho indole synthesis | The Leimgruber-Batcho indole synthesis | Leimgruber-Batcho indole synthesis | 1976 | pharmaceutical industry | drugs | Fischer indole synthesis | The Fischer indole synthesis | Fischer indole synthesis | 1883 | Emil Fischer | Bartoli indole synthesis | Bischler-Möhlau indole synthesis | Fukuyama indole synthesis | Gassman indole synthesis | Hemetsberger indole synthesis | Larock indole synthesis | Madelung synthesis | Nenitzescu indole synthesis | Reissert indole synthesis | dimethyl acetylenedicarboxylate | diphenylhydrazine | xylene | aniline | glacial acetic acid | pyrazolone | pyridine | quinoline | lone pair | electrons | basic | amines | anilines | pKa | hydrochloric acid | protonate | tryptamines | electrophilic aromatic substitution | benzene | Vilsmeier-Haack | formylation | The Vilsmeyer-Haack formylation of indole | Gramine | Mannich reaction | dimethylamine | formaldehyde | Synthesis of Gramine from indole | DMSO | strong bases | sodium hydride | butyl lithium | deprotonation | Salts | ionic | sodium | potassium | electrophiles | covalent | Grignard reagents | zinc | polar | solvents | DMF | DMSO | toluene | Formation and reactions of the indole anion | butyl lithium | lithium diisopropylamide | 2-position lithiation of indole | oxidized | N-bromosuccinimide | oxindole | Oxidation of indole by N-bromosuccinimide | cycloaddition reactions | Diels-Alder reaction | strychnine | diene | dienophile | Example of a cycloaddition of indole | jasmine | oil | perfume | Martinet dioxindole synthesis | Skatole | Stollé synthesis | Tryptamines | ISBN 0-12-676945-1 | ISBN 0-632-05453-0 | ISBN 3-13-112241-2 | ISBN 0-86577-949-X | Baeyer, A. | Baeyer, A. | Chemische Berichte | Chem. Rev. | doi | doi | Chem. Rev. | doi | Chem. Rev. | doi | J. Am. Chem. Soc. | doi | Organic Syntheses | Organic Syntheses | J. Org. Chem. | doi | Org. Lett. | doi | Indole-3-butyric acid | Indole test | Categories | Indoles | Nitrogen heterocycles | Aromatic compounds | Heterocyclic compounds | Simple aromatic rings |
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Indole".