Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000131.xml
Synfacts 2008(10): 1037-1037
DOI: 10.1055/s-2008-1078155
DOI: 10.1055/s-2008-1078155
Synthesis of Heterocycles
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of Benzopyridyloxepines Contain-
ing Stereodefined
Exocyclic Double Bonds
M. W. Carson*, M. W. Giese, M. J. Coghlan
Eli Lilly and Co., Indianapolis, USA
Further Information
Publication History
Publication Date:
22 September 2008 (online)
Significance
Reported is a synthesis of benzopyridyloxepines containing geometrically pure exocyclic tetrasubstituted double bonds. The key steps are 1) a syn-stereoselective diboration of aryl alkynes using bispinacolatodiborane, 2) an intramolecular Suzuki cross-coupling reaction which occurs in stereo- and regiocontrolled fashion and 3) an intermolecular Suzuki-Miyaura cross-coupling to furnish the final tetrasubstituted olefinic benzopyridyloxepines.