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The First Stereoselective Total Synthesis of Quinine Gilbert Stork, Deqiang Niu, A. Fujimoto, Emil R. Koft, James M. Balkovec, James R. Tata, and Gregory R. Dake J. Am. Chem. Soc.; 2001; 123(14) pp 3239 - 3242; (Article) doi:10.1021/ja004325r.
Review: The Woodward-Doering/Rabe-Kindler Total Synthesis of Quinine: Setting the Record Straight Jeffrey I. Seeman Angew. Chem. Int. Ed. 2007, 46, 1378–1413 doi:10.1002/anie.200601551PMID17294412
Communication Rabe Rest in Peace: Confirmation of the Rabe–Kindler Conversion of d-Quinotoxine to Quinine: Experimental Affirmation of the Woodward–Doering Formal Total Synthesis of Quinine Aaron C. Smith, Robert M. Williams Angewandte Chemie International Edition2008, 47, 1736–1740 doi:10.1002/anie.200705421
C–H Activation Enables a Concise Total Synthesis of Quinine and Analogues with Enhanced Antimalarial Activity D. H. O'Donovan et al Angewandte Chemie International Edition 2018doi:10.1002/anie.201804551
Review: The Woodward-Doering/Rabe-Kindler Total Synthesis of Quinine: Setting the Record Straight Jeffrey I. Seeman Angew. Chem. Int. Ed. 2007, 46, 1378–1413 doi:10.1002/anie.200601551PMID17294412
