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. Author manuscript; available in PMC: 2023 Sep 14.
Published in final edited form as: Nature. 2022 Feb 8;604(7904):92–97. doi: 10.1038/s41586-022-04491-w

Extended Data Fig. 9 |. TIDA boronates tolerate a diverse range of cross-coupling chemistry.

Extended Data Fig. 9 |

a, Suzuki–Miyaura cross-coupling. b, Heck coupling. c, Sonogashira coupling. d, Photochemical Suzuki–Miyaura cross-coupling. e, Photochemical thioetherification. f, Stille coupling leading to bis-borylated dienes. g, Stille coupling leading to germylated dienes.