Efficient synthesis of highly hindered dicyanoethylenephenol radical
An efficient and convenient method for the preparation of conjugated and highly sterically hindered dicyanoethylenephenol derivatives was described. The corresponding blue phenoxyl radicals were generated from the oxidation of the dicyanoethylenephenol precursor with alkaline K 3Fe(CN) 6 in benzene.
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Published in | Synthetic metals Vol. 71; no. 1; pp. 1801 - 1802 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
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Elsevier B.V
01.04.1995
Elsevier |
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Abstract | An efficient and convenient method for the preparation of conjugated and highly sterically hindered dicyanoethylenephenol derivatives was described. The corresponding blue phenoxyl radicals were generated from the oxidation of the dicyanoethylenephenol precursor with alkaline K
3Fe(CN)
6 in benzene. |
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AbstractList | An efficient and convenient method for the preparation of conjugated and highly sterically hindered dicyanoethylenephenol derivatives was described. The corresponding blue phenoxyl radicals were generated from the oxidation of the dicyanoethylenephenol precursor with alkaline K3Fe(CN)(6) in benzene. An efficient and convenient method for the preparation of conjugated and highly sterically hindered dicyanoethylenephenol derivatives was described. The corresponding blue phenoxyl radicals were generated from the oxidation of the dicyanoethylenephenol precursor with alkaline K 3Fe(CN) 6 in benzene. |
Author | Upasani, R.B. Chiang, L.Y. Wang, Lee Y. |
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Title | Efficient synthesis of highly hindered dicyanoethylenephenol radical |
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