Summary.
The reactive 1:1 intermediate produced in the reaction between dialkyl acetylenedicarboxylates and triphenylphosphine was trapped by ethyl 3-(1,2-dihydroquinoline-2-ylidene)-pyruvate to yield the isomeric dialkyl 3-ethoxy-4-oxo-5-(2-(1H)-quinolinylidene)-2-cyclopentene-1,2-dicarboxylates and trialkyl 4-(2-quinolyl)-1-cyclobutene-1,2,3-tricarboxylates in nearly 4:1 ratio.
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Received April 3, 2001. Accepted (revised) May 22, 2001
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Yavari, I., Adib, M. & Esnaashari, M. Vinylphosphonium Salt Mediated Facile Synthesis of Trialkyl 4-(2-Quinolyl)-1-cyclobutene-1,2,3-tricarboxylates and Dialkyl 3-Ethoxy-4-oxo-5-(2-(1H)-quinolinylidene)-2-cyclopentene-1,2-dicarboxylates. Monatshefte für Chemie 132, 1557–1561 (2001). https://doi.org/10.1007/s007060170013
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DOI: https://doi.org/10.1007/s007060170013