Solventless lactam synthesis by intramolecular cyclizations of α-iminoester derivatives under microwave irradiation

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Abstract

We have previously reported a new synthesis of amides from esters and amines under microwave irradiation, offering much higher yields than those achieved with conventional heating [1]. We have now extended these studies to the ring closure of neat iminoesters I2, I3 and I4-I6 to give five- and six-membered ring lactams L5, L6 and larger lactams L7-L9 (where I means imine and L means lactam), respectively, under both classical heating conditions and microwave irradiation. © 2007 by MDPI.

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Zradni, F. Z., Hamelin, J., & Derdour, A. (2007). Solventless lactam synthesis by intramolecular cyclizations of α-iminoester derivatives under microwave irradiation. Molecules, 12(3), 439–454. https://doi.org/10.3390/12030439

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