In a new study published in Nature Communications, a team of chemists has unveiled a radically simple way to attach a highly sought-after “molecular handle,” known as the dichloromethyl group, onto complex compounds. Instead of relying on the aggressive, heavy-metal or radiation-heavy techniques of the past, the team used a common, naturally occurring amino acid called proline to gently choreograph the assembly.

“Rather than forcing these molecules into conventional reactivity modes or circumventing their electronic ambivalence, we harnessed their electronic ambivalence as a design principle,” says Prof. Dmitry Tsvelikhovsky, who led the research team at the Institute for Drug Research at the Hebrew University, alongside Elihay Kuniavsky and Dvora R. Levy.