Halogenation of N-substituted p-quinone monoimines and p-quinone monooxime ethers: XIV. Halogenation of N-[arylsulfonylimino(phenyl)methyl]-2,5-dialkyl-1,4-benzoquinone monoimines and their reduction products |
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Authors: | A. P. Avdeenko S. A. Konovalova O. P. Ledeneva A. A. Santalova V. V. Pirozhenko G. V. Palamarchuk O. V. Shishkin |
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Affiliation: | 1. Donbass State Engineering Academy, ul. Shkadinova 72, Kramatorsk, 84313, Ukraine 2. Institute of Organic Chemistry, National Academy of Sciences of Ukraine, ul. Murmanskaya 5, Kiev, 02660, Ukraine 3. Institute of Single Crystals, National Academy of Sciences of Ukraine, Kharkiv, Ukraine 4. Karazin Kharkiv National University, Kharkiv, Ukraine
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Abstract: | Despite steric hindrances created by the bulky substituent on the nitrogen atom, halogenation of 2,5-dialkyl-N-[arylsulfonylimino(phenyl)methyl]-1,4-benzoquinone monoimines fairly readily gives their derivatives having two halogen atoms in the quinoid ring. |
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