- rearomatization
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Any reaction in which an aromatic compound, that had been converted into a non-aromatic one, is reconverted to an aromatic one.See Also: rearomatize
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rearomatization
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Diels-Alder reaction — The Diels Alder reaction is an organic chemical reaction (specifically, a cycloaddition) between a conjugated diene and a substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene system. [cite journal author = Diels,… … Wikipedia
Doebner-Miller reaction — The Doebner Miller reaction is the organic reaction of an aniline with α,β unsaturated carbonyl compounds to form quinolines. [Doebner, O.; Miller, W. v. Ber. 1881, 14 , 2812.] [Doebner, O.; Miller, W. v. Ber. 1883, 16 , 1664 2464.] [Doebner, O.; … Wikipedia
Wagner-Jauregg reaction — The Wagner Jauregg reaction is a classic organic reaction in organic chemistry, named after Theodor Wagner Jauregg, describing the Diels Alder reaction of 2 equivalents of maleic anhydride with a 1,1 diarylethylene. After aromatization of the bis … Wikipedia
Cyclopropanone — IUPAC name cyclopropanone Identifie … Wikipedia
rearomatize — verb To cause, or to undergo rearomatization … Wiktionary
rearomatizing — adjective Causing or undergoing rearomatization … Wiktionary
Diels–Alder reaction — Named after Otto Paul Hermann Diels Kurt Alder Reaction type Cycloaddition Reaction … Wikipedia
Doebner–Miller reaction — The Doebner Miller reaction is the organic reaction of an aniline with α,β unsaturated carbonyl compounds to form quinolines.[1][2][3][4] … Wikipedia
Organogold chemistry — is the study of compounds containing carbon gold bonds. They are studied in academic research, but have not received widespread use otherwise. The dominant oxidation states for organogold compounds are I with coordination number 2 and a linear… … Wikipedia
