4.8 Article

Palladium-Catalyzed Sequential Cyanation/N-Addition/N-Arylation in One-Pot: Efficient Synthesis of Luotonin A and Its Derivatives

Journal

ORGANIC LETTERS
Volume 11, Issue 16, Pages 3582-3585

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol901305q

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Funding

  1. National Natural Science Foundation of China [20672136, 20702060, 20832006)]
  2. Shanghai Municipal Committee of Science and Technology [07XD14038]

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With the catalysis of palladium, a number of 2-bromo-N-(2-iodobenzyl)benzamides underwent sequential cyanation/N-addition/N-arylation leading to the efficient construction of isoindolo[1,2-b]quinazolin-10(12H)-ones in a two-stage, one-pot manner. This method also allowed the convenient synthesis of luotonin A and its derivatives.

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