Linsenmeier, Anna M.; Williams, Craig M.; Brase, Stefan published an article in 2013, the title of the article was Photochemical Synthesis of Phenanthridines: Exploring Fluoro and Protected Catechol Substitution.Name: 1-(Bromomethyl)-4-fluoro-2-iodobenzene And the article contains the following content:
Substituted phenanthridines, such as the natural product trispheridine, have been accessed by the practical photochem. cyclization of N-benzylanilines. Functionalities, with a focus on fluoro substituents and protected catechols, are well tolerated on both the A and C rings. The phenanthridines were accessed in good to very good yields (up to 95 %) from iodinated substrates, whereas brominated substrates performed poorly in comparison (0-48 %). The experimental process involved the reaction of 1-(Bromomethyl)-4-fluoro-2-iodobenzene(cas: 70931-59-8).Name: 1-(Bromomethyl)-4-fluoro-2-iodobenzene
The Article related to iodobenzylaniline fluoro protected catechol containing photochem cyclization, phenanthridine preparation, Heterocyclic Compounds (One Hetero Atom): Other Areno- and Diarenopyridines (Acridines, Quinolizines, etc.) and other aspects.Name: 1-(Bromomethyl)-4-fluoro-2-iodobenzene
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com