Stereospecific synthesis of trans-5,6-dihydropyridinones was written by Chou, Shang-Shing P.;Yang, Tsung-Han;Wu, Wan-Shiuan;Chiu, Tzu-Han. And the article was included in Synthesis in 2011.Recommanded Product: 1-Chloro-4-iodobutane This article mentions the following:
An efficient synthesis of trans-5,6-dihydropyridinones bearing a heteroatom (Br, OH) at C(5) was achieved. The formal synthesis of (±)-epiquinamide and (±)-homopumiliotoxin 223G was also accomplished through the formation of (±)-trans-1-hydroxyquinolizidin-4-one. In the experiment, the researchers used many compounds, for example, 1-Chloro-4-iodobutane (cas: 10297-05-9Recommanded Product: 1-Chloro-4-iodobutane).
1-Chloro-4-iodobutane (cas: 10297-05-9) belongs to iodide derivatives. Iodide-containing intermediates are common in organic synthesis, because of the easy formation and cleavage of the C–I bond. A typical method for synthesis of aromatic iodides is diazotization of primary aromatic amines followed by treatment of potassium iodide. Aliphatic alcohols are converted to alkyl iodides by treating with hydrogen iodide.Recommanded Product: 1-Chloro-4-iodobutane
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com