Figure 1: Advances in the Suzuki–Miyaura cross-coupling reaction. | Nature Communications

Figure 1: Advances in the Suzuki–Miyaura cross-coupling reaction.

From: Iterative protecting group-free cross-coupling leading to chiral multiply arylated structures

Figure 1

(a) Classical Suzuki–Miyaura reaction for the formation of C–C bonds between aryl or alkenyl electrophiles and aryl or alkenyl organoboron nucleophiles. (b) Selected examples of molecules prepared by enantiospecific Suzuki–Miyaura cross-coupling reactions. (c) Iterative coupling concept employing the Suzuki–Miyaura reaction as the key structure-building component. (d) This work: chemoselective, protecting group-free cross-coupling of multiply borylated organic compounds, including the coupling of chiral, enantioenriched B–C bonds.

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