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Publikováno v:
Vìsnik Odesʹkogo Nacìonalʹnogo Unìversitetu: Hìmìâ, Vol 22, Iss 1(61), Pp 103-118 (2017)
The hydrohalogenation of N-arylaminocarbonyl-1,4-benzoquinone monoimines is optimal method to obtain the halogenated derivatives. This method allows obtaining the pure products in high yield with a halogen atom in the aminophenol ring. The brominatio
Externí odkaz:
https://doaj.org/article/918850d0747e48c1abf71bec574a2d66
Publikováno v:
Vìsnik Odesʹkogo Nacìonalʹnogo Unìversitetu: Hìmìâ, Vol 22, Iss 1(61), Pp 103-118 (2017)
The hydrohalogenation of N-arylaminocarbonyl-1,4-benzoquinone monoimines is optimal method to obtain the halogenated derivatives. This method allows obtaining the pure products in high yield with a halogen atom in the aminophenol ring. The brominatio
Publikováno v:
Odesa National University Herald. Chemistry; Том 22, № 1(61) (2017); 103-118
Вестник Одесского национального университета. Химия; Том 22, № 1(61) (2017); 103-118
Вісник Одеського національного університету. Хімія; Том 22, № 1(61) (2017); 103-118
Вестник Одесского национального университета. Химия; Том 22, № 1(61) (2017); 103-118
Вісник Одеського національного університету. Хімія; Том 22, № 1(61) (2017); 103-118
The hydrohalogenation of N-arylaminocarbonyl-1,4-benzoquinone monoimines is optimal method to obtain the halogenated derivatives. This method allows obtaining the pure products in high yield with a halogen atom in the aminophenol ring. The brominatio