4.4 Article

Synthesis of the tetracyclic core skeleton of the lundurines by a gold-catalyzed cyclization

Journal

TETRAHEDRON
Volume 65, Issue 44, Pages 9015-9020

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2009.08.067

Keywords

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Funding

  1. MICINN [CrQ2007-60745/BQU]
  2. Consolider Ingenio 2010 [CSD2006-0003]
  3. AGAUR
  4. ICIQ Foundation

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The 1H-azocino[5,4-b]indole skeleton of the lundurines has been prepared by the 8-endo-dig cyclization of an alkynylindole using AuCl3 or other gold complexes as catalysts. (C) 2009 Elsevier Ltd. All rights reserved.

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