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. Author manuscript; available in PMC: 2014 Oct 7.
Published in final edited form as: Nat Commun. 2014 Apr 7;5:3470. doi: 10.1038/ncomms4470

Fig. 3.

Fig. 3

The reaction scope with isolated yields reported. (A) Reactions of various acids with 1-hexyne or 1-dodecyne. (B) Reactions of various alkynes with benzoic acid. Reactions run under N2 in vial. NaBARF, sodium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate.