An Efficient Synthetic Route to Novel 3-Alkyl- and 3-Aryl-4-iodophenols
Autor: | Lucía Díaz, Marta Corrales, Hermann Gesine Johanna, Robert Alan Goodnow, Peter D. Edwards, Michael C. Annis |
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Rok vydání: | 2008 |
Předmět: | |
Zdroj: | Synthesis. 2008:221-224 |
ISSN: | 1437-210X 0039-7881 |
Popis: | An efficient method for the preparation of novel 3-alkyl- and 3-aryl-4-iodophenols from 3-alkyl- and 3-arylphenols is de- scribed. As part of an ongoing project it was necessary to access a series of novel 4-arylphenols containing sterically de- manding functionality at the 3-position; in particular phe- nols with isopropyl, tert-butyl, and phenyl groups were of interest for our work. A viable approach to these com- pounds via palladium-catalysed coupling of the 3-alkyl- and 3-aryl-4-halophenols 1 (Figure 1) was proposed. However, literature searches revealed a paucity of infor- mation regarding the synthesis of these 4-halogenated 3- alkyl- and 3-arylphenols. |
Databáze: | OpenAIRE |
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