Efficient Synthesis of 3‐Pyrrolylquinolines via an 1,3‐Dipolar Cycloaddition/Oxidation Sequence |
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| Authors: | H Menasra A Kedjadja A Debache S Rhouati Bertrand Carboni |
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| Institution: | 1. Laboratoire des Produits Naturels d'Origine Végétalé et de Synthèse Organique , Faculté des Sciences, Campus de Chaabat Ersas, Université Mentouri‐Constantine , Algérie;2. Organométalliques et Catalyse , UMR 6509, Institut de Chimie, Université de Rennes I, Campus de Beaulieu , Rennes Cedex , France |
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| Abstract: | The synthesis of some new functionalized quinolyl derivatives relies on the 1,3‐dipolar cycloaddition of an azomethine ylide, generated from sarcosine and paraformaldehyde, to quinolyl α,β‐unsaturated esters, followed by oxidation of the pyrrolidinyl moiety to pyrrole with activated MnO2. |
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| Keywords: | Dipolar cycloaddition oxidation pyrroles quinolines Wittig reaction |
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