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. Author manuscript; available in PMC: 2016 Oct 20.
Published in final edited form as: Eur J Med Chem. 2015 Aug 29;103:226–237. doi: 10.1016/j.ejmech.2015.08.047

Figure 2.

Figure 2

(A) Demonstration of the feasibility of the modified Paal-Knorr condensation of 1 to form pyrrole 2, (B) Paal-Knorr pyrrole formation implicated in the neurotoxicity of hexane and (C) novel pyrrolylation of primary amines with C12-Wittig derivatives reported herein.