In 2019,Chemistry – A European Journal included an article by Virelli, Matteo; Wang, Wei; Kuniyil, Rositha; Wu, Jun; Zanoni, Giuseppe; Fernandez, Antonio; Scott, Jamie; Vendrell, Marc; Ackermann, Lutz. Category: iodides-buliding-blocks. The article was titled 《BODIPY-Labeled Cyclobutanes by Secondary C(sp3)-H Arylations for Live-Cell Imaging》. The information in the text is summarized as follows:
Arylated cyclobutanes were accessed by a versatile palladium-catalyzed secondary C(sp3)-H activation, exploiting chelation assistance by modular triazoles. The C-H arylation led to cyclobutane natural product derivatives in a highly regioselective fashion, setting the stage for the easy access to novel fluorogenic boron-dipyrrin (BODIPY)-labeled probes for live-cell imaging.1-Chloro-3-iodobenzene(cas: 625-99-0Category: iodides-buliding-blocks) was used in this study.
1-Chloro-3-iodobenzene(cas: 625-99-0) belongs to organic iodides. The carbon-iodine bond is weaker than other carbon-halogen bonds due to the poor electronegative nature of the iodine atom. Category: iodides-buliding-blocks Alkyl iodides react at a faster rate than alkyl fluorides due to the weak C-I bond.
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com