4.4 Article

Total synthesis of (±)-13-epineostenine

Journal

TETRAHEDRON
Volume 65, Issue 29-30, Pages 5716-5719

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2009.05.022

Keywords

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Funding

  1. NSFC [20621091, 20672048, 20732002]
  2. '111' program of Chinese Education Ministry.

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An efficient total synthesis of (+/-)-13-epineostenine (2) has been achieved in 15 steps and 17% overall yield. This approach involved the key alkylation/Michael additions of the central 1,4-cyclohexanedione monoethylene acetal and all of the stereocenters on central cyclohexane moiety were generated in highly stereoselectivity. (C) 2009 Elsevier Ltd. All rights reserved.

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