4.8 Article

Asymmetric Synthesis of Cyclopenta[3,4]pyrroloindolones via N-Heterocyclic Carbene-Catalyzed Michael/AIdoI/Lactamization Cascade Reaction

Journal

ORGANIC LETTERS
Volume 19, Issue 12, Pages 3271-3274

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b01411

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Funding

  1. National Natural Science Foundation [21372106]
  2. Program 111

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The N-heterocyclic carbene-catalyzed asymmetric Michael/aldol/lactamization cascade reaction of enals and indole-derived enones for the synthesis of functionalized cyclopenta[3,4]pyrroloindolones with four consecutive stereogenic centers has been achieved. The products were obtained in good yield with high diastereoselectivity and excellent enantioselectivity.

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