Autor: |
Anselmi, Elsa, Bahlaouan, Zineb, Inack Ngi, Samuel, Parrain, Jean Luc, Magnier, Emmanuel, Abarbri, Mohamed |
Předmět: |
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Zdroj: |
European Journal of Organic Chemistry; 11/9/2017, Vol. 2017 Issue 41, p6131-6136, 6p |
Abstrakt: |
A facile, and totally regioselective one-pot approach to synthesize 5,7-diiodo-3-substituted-isocoumarins is described. This reaction was realized by using copper iodide as the catalyst under mild reaction conditions. The methodology was used to design a wide variety of compounds and was tolerant to a large number of functional groups. Interestingly, among the three possible carbon-iodine bonds, only one was reactive, which left the two others intact for further functionalization. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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