Renate Kristianslund, Jørn Eivind Tungen and Trond Vidar Hansen
Org. Biomol. Chem., 2019,17, 3079-3092
DOI:
10.1039/C8OB03160F,
Review Article
The halolactonization reaction is a useful chemical transformation for the construction of lactones from γ- or δ-substituted alkenoic carboxylic acids or carboxylic esters. Traditionally, the stereoselectivity of these reactions has been controlled by the substrates or the reagents. The substrate-controlled method has been extensively studied and applied in the synthesis of many natural products. However, catalytic, enantioselective iodolactonizations of γ- or δ-substituted alkenoic carboxylic acids have only recently been developed. This review article highlights the advances that have emerged over the last decade.