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. 2016 Aug 9;8(1):165–168. doi: 10.1039/c6sc02668k

Fig. 1. Kinetic profiles of the formation of B1 using various catalytic systems. [a] Reactions were carried out in a J-Young NMR tube at RT under an argon atmosphere using a 1 : 1 mixture (0.45 mmol) of p-tolylacetylene and pinacolborane in 1 mL of C6D6. [b] 2.5 mol% of F and 5 mol% Et3N; no trace of B1 was observed, instead D1 was obtained quantitatively. [c] 2.5 mol% of F, Et3N and Et3NH·OTf. [d] 2.5 mol% of A, 3.75 mol% Et3N and 1.25 mol% Et3NH·OTf. [e] 2.5 mol% of L1CuOTf and 5 mol% of Et3N.

Fig. 1