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. 2018 May 21;9(23):5295–5300. doi: 10.1039/c8sc01355a

Fig. 2. Synthesis of 1-iodo- and 1-bromo-3-substituted BCPs. All reactions performed using 2 equiv. tricyclo[1.1.1.01,3]pentane (TCP) and 10 mol% BEt3 (1 M in hexane) at room temperature, unless indicated otherwise. a1.1 equiv. TCP, 1 mol% BEt3, 0 °C. b1.3 equiv. TCP, rt. c1.3 equiv. TCP, 0 °C. dCo-solvent added to solubilize the substrate: MeOH for 5m, n; CH2Cl2 for 5h, k, r and 6e, f. e5% staffane observed.

Fig. 2