Concise Total Synthesis of Permethylated Anigopreissin A, a New Benzofuryl Resveratrol Dimer was written by Chiummiento, Lucia;Funicello, Maria;Lopardo, Maria Teresa;Lupattelli, Paolo;Choppin, Sabine;Colobert, Francoise. And the article was included in European Journal of Organic Chemistry in 2012.Recommanded Product: Methyl 3,5-dihydroxy-4-iodobenzoate This article mentions the following:
The versatile preparation of permethylated anigopreissin A (1) has been accomplished from Me 3,5-dihydroxybenzoate. The key steps of the synthesis are sequential Sonogashira and Suzuki cross-couplings for the construction of the 2,3-diarylbenzo[b]furan moiety and Wittig olefination for the introduction of the styryl group. In the experiment, the researchers used many compounds, for example, Methyl 3,5-dihydroxy-4-iodobenzoate (cas: 338454-02-7Recommanded Product: Methyl 3,5-dihydroxy-4-iodobenzoate).
Methyl 3,5-dihydroxy-4-iodobenzoate (cas: 338454-02-7) belongs to iodide derivatives. Organic iodides are widely used in organic synthesis. Halogenation of aromatic hydrocarbons is a very important reaction via an electrophilic aromatic substitution. Alkyl iodides react at a faster rate than alkyl fluorides due to the weak C-I bond.Recommanded Product: Methyl 3,5-dihydroxy-4-iodobenzoate
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com