《Alkyl Tosylates as Alkylating Reagents in the Catellani Reaction》 was published in Synthesis in 2020. These research results belong to Gao, Qianwen; Liu, Ze-Shui; Hua, Yu; Zhou, Siwei; Cheng, Hong-Gang; Zhou, Qianghui. Recommanded Product: 1-Iodonaphthalene The article mentions the following:
A cooperative catalytic system involving a Pd/XPhos complex and inexpensive 5-norbornene-2-carbonitrile that enabled the use of alkyl tosylates as alkylating reagents in the Catellani reaction was developed. This mild, scalable protocol was compatible with a range of readily available functionalized aryl iodides and alkyl tosylates, as well as terminating olefins (45 examples, up to 97% yield). The experimental part of the paper was very detailed, including the reaction process of 1-Iodonaphthalene(cas: 90-14-2Recommanded Product: 1-Iodonaphthalene)
1-Iodonaphthalene(cas: 90-14-2) is one of organic iodides. Organic iodides are used in veterinary products (Organic Iodide Powder) as a nutritional source of iodine. In the chemical industry, alkyl iodides serve as excellent alkylating agents and, specifically, methyl iodide is used as a methylating agent in the synthesis of various pharmaceutical drugs. Oceanic alkyl iodides are believed to be the principal source of atmospheric iodine.Recommanded Product: 1-Iodonaphthalene
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com