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  2. Birch reduction - Wikipedia

    en.wikipedia.org/wiki/Birch_reduction

    Birch reduction of benzene, also available in animated form. The reaction is known to be third order – first order in the aromatic, first order in the alkali metal, and first order in the alcohol. [4] This requires that the rate-limiting step be the conversion of radical anion B to the cyclohexadienyl radical C. Birch reduction of anisole.

  3. Anisole - Wikipedia

    en.wikipedia.org/wiki/Anisole

    Anisole, or methoxybenzene, is an organic compound with the formula CH 3 OC 6 H 5. ... Birch reduction of anisole gives 1-methoxycyclohexa-1,4-diene. [6] Synthesis

  4. Cyclohexenone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexenone

    Cyclohexenone is obtained by Birch reduction of anisole followed by acid hydrolysis. It can be obtained from cyclohexanone by α-bromination followed by treatment with base. Hydrolysis of 3-chloro cyclohexene followed by oxidation of the cyclohexenol is yet another route.

  5. Solvated electron - Wikipedia

    en.wikipedia.org/wiki/Solvated_electron

    Tetrahydrofuran (THF) dissolves alkali metal, but a Birch reduction (see § Applications) analogue does not proceed without a diamine ligand. [8] Solvated electron solutions of the alkaline earth metals magnesium, calcium, strontium and barium in ethylenediamine have been used to intercalate graphite with these metals. [9]

  6. Organoiron chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoiron_chemistry

    Cyclohexadienes, many derived from Birch reduction of aromatic compounds, form derivatives (diene)Fe(CO) 3. The affinity of the Fe(CO) 3 unit for conjugated dienes is manifested in the ability of iron carbonyls catalyse the isomerisations of 1,5-cyclooctadiene to 1,3-cyclooctadiene. Cyclohexadiene complexes undergo hydride abstraction to give ...

  7. Betti reaction - Wikipedia

    en.wikipedia.org/wiki/Betti_reaction

    The reaction is named after the Italian chemist Mario Betti (1857-1942). Betti worked at many universities in Italy, including Florence, Cagliari, Siena, Genoa and Bologna, where he was the successor of Giacomo Ciamician.

  8. Danheiser benzannulation - Wikipedia

    en.wikipedia.org/wiki/Danheiser_Benzannulation

    Scheme 1: Danheiser Benzannulation Reaction of an Alkyne and a Cyclobutenone(X= OR, SR, NR2) The Danheiser benzannulation is a regiocontrolled phenol annulation. This annulation provides an efficient route to form an aromatic ring in one step. [5]

  9. 2,4,6-Tribromoanisole - Wikipedia

    en.wikipedia.org/wiki/2,4,6-Tribromoanisole

    2,4,6-Tribromoanisole (TBA) is a chemical compound that is a brominated derivative of anisole. It is one of the chemicals responsible for cork taint. [2] Tribromoanisole is a fungal metabolite of 2,4,6-tribromophenol, which is used as a fungicide. It can be found in minute traces on packaging materials stored in the presence of fiberboard ...