tetralone

tetralone
Either of two isomers of the bicyclic ketone benzocyclohexanone containing a benzene ring fused with that of cyclohexanone; it is use in the synthesis of other compounds, especially the contraceptive 18-methyl norethisterone

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  • tetralone — tet·ra·lone …   English syllables

  • tetralone — ˈte.trəˌlōn noun ( s) Etymology: International Scientific Vocabulary tetralin + one : either of two ketones C10H10O derived from tetrahydronaphthalene …   Useful english dictionary

  • Sodium bisulfite — Sodium bisulfite …   Wikipedia

  • Friedel-Crafts reaction — The Friedel Crafts reactions are a set of reactions developed by Charles Friedel and James Crafts in 1877. [Friedel, C.; Crafts, J. M. Compt. Rend. 1877, 84 , [http://gallica.bnf.fr/ark:/12148/bpt6k30410/f1386.table 1392]… …   Wikipedia

  • Bucherer reaction — The Bucherer reaction in organic chemistry is the reversible conversion of Naphthol to naphtylamine in presence of ammonia and sodium bisulfite [ H Bucherer. Journal für Praktische Chemie 49 (1904) p69] [ H Seeboth. Angew Chem Int Ed 6(4) (1967)… …   Wikipedia

  • Коптюг — Коптюг, Валентин Афанасьевич Валентин Афанасьевич Коптюг Дата рождения: 9 июня 1931(1931 06 09) Место рождения: Юхнов, Западная область, СССР Дата смерти: 10 января 1997 …   Википедия

  • scytalone — noun A tetralone derivative involved in certain redox reactions …   Wiktionary

  • Friedel–Crafts reaction — The Friedel–Crafts reactions are a set of reactions developed by Charles Friedel and James Crafts in 1877.[1] There are two main types of Friedel–Crafts reactions: alkylation reactions and acylation reactions. This reaction type is a form of… …   Wikipedia

  • 5,8-Dihydroxy-1,4-naphthoquinone — 5,8 Dihydroxy 1,4 naphthoquinone …   Wikipedia

  • Réaction de Bucherer — La réaction de Bucherer est une réaction organique réversible qui permet de convertir un naphtol en naphtylamine par réaction avec l ammoniaque et le bisulfite de sodium[1],[2],[3] …   Wikipédia en Français

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