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Migratory Insertion Strategies for Dearomatization

Journal

SYNTHESIS-STUTTGART
Volume 51, Issue 22, Pages 4137-4146

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0037-1611918

Keywords

palladium; nickel; dearomatization; migratory insertion; carbopalladation; difunctionalization

Funding

  1. Natural Sciences and Engineering Research Council (NSERC)
  2. University of Toronto
  3. Alphora Research Inc.
  4. Kennarshore Inc.
  5. province of Ontario

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Development of strategies for molecule functionalization by dearomatization has surged in the last two decades. The benefits of overcoming the resonance stabilization energy outweigh the cost; diverse compounds could be accessed in a short number of steps. One approach that has been of interest in recent years is the dearomatization of indoles and other (hetero)aromatic compounds by migratory insertion. The chiral sigma-bond palladium intermediate could be reduced or trapped by a second functionalization. In this short review we will summarize the recently discovered reactions from our group and others in this field of metal-catalyzed dearomatizations by migratory insertion. 1 Introduction 2 Monofunctionalizations: Heck and Reductive Heck Reactions 2.1 N -Tethered Heterocycles 2.2 Non- N -tethered Heterocycles 2.3 Non-heterocycles 3 Dearomative Difunctionalizations: Interrupted Heck Reaction 3.1 N -Tethered Heterocycles 3.2 Non- N -tethered Heterocycles 4 Conclusion

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