Some scientific research tips on 60827-45-4

In some applications, this compound(60827-45-4)Product Details of 60827-45-4 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 60827-45-4, is researched, SMILESS is OC[C@H](O)CCl, Molecular C3H7ClO2Journal, Heterocycles called A formal synthesis of (+)-α-allokainic acid via sulfanyl radical addition-cyclization reaction, Author is Miyata, Okiko; Ozawa, Yoshiki; Ninomiya, Ichiya; Aoe, Keiichi; Hiramatsu, Hajime; Naito, Takeaki, the main research direction is allokainic acid total synthesis radical cyclization; sulfanyl radical addition cyclization diallylamine; pyrrolidine preparation radical addition cyclization diallylamine.Product Details of 60827-45-4.

Sulfanyl radical addition-cyclization of diallylamine I in the presence of thiophenol and AIBN gave the 2,3,4-trisubstituted pyrrolidines II (R = PhSCH2, R1 = H; R = H, R1 = PhSCH2) which were effectively converted into the known key intermediate for the synthesis of (+)-α-allokainic acid via conversion of the phenylsulfanylmethyl group into the isopropenyl group at the 4-position.

In some applications, this compound(60827-45-4)Product Details of 60827-45-4 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com