4.7 Article

Cascade Synthesis of 3-Quinolinecarboxylic Ester via Benzylation/Propargylation-Cyclization

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 73, Issue 21, Pages 8608-8611

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo8017654

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Funding

  1. Natural Science Foundation of China [20629202]
  2. Chinese Academy of Sciences

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Reactions of 2-amino-aryl alcohols with beta-ketoesters catalyzed by a catalytic amout of FeCl3 via tandem benzylation-cyclization produce the corresponding 3-quinolinecarboxylic esters in good to high yields. Extending this methodology to propargylation-cyclization, 2-nitrophenyl proparoyl alcohols with beta-ketoesters catalyzed by FeCl3 and SnCl, also produce the 4-alkyne-3-quitiolinecarboxylic esters. The mechanistic details of this benzylation/proparoylation and cyclization cascade process are also discussed.

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