solventless lactam synthesis by intramolecular cyclizations of α-iminoester derivatives under microwave irradiation不溶解的内酰胺合成的分子内环合α-iminoester微波辐照下衍生品.pdfVIP
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solventless lactam synthesis by intramolecular cyclizations of α-iminoester derivatives under microwave irradiation不溶解的内酰胺合成的分子内环合α-iminoester微波辐照下衍生品
Molecules 2007, 12, 439-454
molecules
ISSN 1420-3049
Full Paper
Solventless Lactam Synthesis by Intramolecular Cyclizations of
α-Iminoester Derivatives under Microwave Irradiation
Fatima-Zohra Zradni 1,*, Jack Hamelin 2 and Aicha Derdour 1,†
1 Faculté des Sciences, Département de Chimie, Université d’Es-sénia, Oran, B.P 1524, Algeria;
†E-Mail: derdouraicha@yahoo.fr
2 Groupe dIngénierie Chimique et Molécules pour le Vivant 3(ICMV3)-UMR 6226, Université de
Rennes 1, Campus de Beaulieu, 35042 Rennes, France; E-mail: jack.hamelin@orange.fr
* Author to whom correspondence should be addressed; E-mail: fzradnidz@yahoo.fr; Tel/Fax: (+213)
41 58 70 57
Received: 27 January 2007; in revised form: 17 February 2007 / Accepted: 7 March 2007 /
Published: 12 March 2007
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.
Keywords: Medium-sized ring lactams; imine alkylation; Schiff bases; microwave
irradiation.
Introduction
Lactams are of considerable interest in a number of areas, ranging from drug discovery to the
polymer industry, and consequently their synthesis has been, and
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