4.6 Article

Synthetic Approaches to Tricyclic Aminoketones in the Total Synthesis of Aspidosperma and Kopsia Alkaloids

Journal

CHEMICAL RECORD
Volume 21, Issue 2, Pages 295-314

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/tcr.202000131

Keywords

tricyclic aminoketones; aspidosperma alkaloids; kopsia alkaloids; total synthesis; synthetic approaches

Funding

  1. NSFC [21971065, 21722202, 21672069]
  2. STCSM [20XD1421500, 20JC1416800, 18JC1415600]
  3. Innovative Research Team of High-Level Local Universities in Shanghai [SSMU-ZLCX20180501]
  4. Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning

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Aspidosperma and kopsia alkaloids are important functional molecules with potent biological activities. Their complex structures pose a synthetic challenge but have attracted significant attention from the synthetic organic academic community. A series of elegant synthetic strategies have been developed, with Stork's original Fischer indolization being particularly noteworthy.
Aspidosperma and kopsia alkaloids are significant functional molecules because of their potent biological activities. Their intricate structures present an intrinsic synthetic challenge and thus attract significant attention from synthetic organic academic community. Over the past decades, a series of elegant strategies has been developed, in particular, the Stork's original Fischer indolization of tricyclic aminoketones 1. Herein, we report a comprehensive review on various synthetic approaches access to tricyclic aminoketones 1 and provide a practical guidance to readers whose are interested in employing tricyclic aminoketones 1 as versatile building blocks in the realm of total synthesis of aspidosperma, kopsia and structurally related alkaloids.

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