Published in
Royal Society of Chemistry, Organic and Biomolecular Chemistry, 2(15), p. 408-415
DOI: 10.1039/c6ob02587k
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Universal access to megastigmanes through controlled cyclisation towards highly substituted cyclohexenes
Journal article published in 2017 by
José A. González-Delgado,
Miguel A. Romero,
Uwe Pischel,
Jesús F. Arteaga 
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Abstract
Efficient few-step asymmetric synthesis of tectoionol B, a representative member of the megastigmane family, starting from geranylacetone via ZrCl4-mediated selective formation of the highly substituted cyclohexene skeleton.