Oxidation of Dimedone by Hydrobromic Acid in Dimethylsulfoxide and Synthesis of 3,5-Dibromo-2,6-dihydroxy-4,4-dimethyl-2,5-cyclohexadien-1-one and 3,5,5-Tribromo-4,4-dimethyl-2-hydroxy-2-cyclopenten-1-one

Oxidation of Dimedone by Hydrobromic Acid in Dimethylsulfoxide and Synthesis of 3,5-Dibromo-2,6-dihydroxy-4,4-dimethyl-2,5-cyclohexadien-1-one and 3,5,5-Tribromo-4,4-dimethyl-2-hydroxy-2-cyclopenten-1-one

Bibliografske podrobnosti
Parent link:	Russian Journal of Organic Chemistry.— , 1965- Vol. 33, iss. 2.— 1997.— P. 158-160
Drugi avtorji:	Yusubov M. S. Mekhman Suleiman-Ogly (Suleimanovich), Zholobova G. A., Habicher W., Filimonov V. D. Viktor Dmitrievich
Izvleček:	Hydrogen bromide in DMSO oxidizes dimedone differently than known cyclic β-diketones: 3,5-dibromo-2,6-dihydroxy-4,4-dimethyl-2,5-cyclohexadien-1-one and 3,5,5-tribromo-4,4-dimethyl-2-hydroxy-2-cyclopenten-1-one are formed instead of vicinal triketones. В фонде НТБ ТПУ отсутствует
Jezik:	angleščina
Izdano:	1997
Teme:	труды учёных ТПУ
Format:	Book Chapter
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=596552

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