4.6 Article

Total Synthesis and Stereochemical Assignment of Actinoranone

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 23, 期 15, 页码 3572-3576

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201700476

关键词

actinoranone; meroterpenoid; natural products; stereochemistry; total synthesis

资金

  1. Shenzhen Peacock Plan [KQTD2015071714043444]
  2. NSFC [21572007, 21272011, 21133002]
  3. SZSTDF [JCYJ20160527100424909, JCYJ20150629144022829, JSGG 20160608091824706, 20140717102922014]
  4. GDNSF [2014A030312004, 2014B030301003]
  5. Fong Shu Fook Tong Foundation
  6. Joyce M. Kuok Foundation

向作者/读者索取更多资源

The total synthesis of four actinoranone stereoisomers led to unambiguous assignment of relative and absolute stereochemistry of the natural product. Key features of the convergent, fully stereocontrolled route include the use of a Negishi carbozirconation/iodination, a Friedel-Crafts cyclization, a Felkin-controlled addition reaction, a Mitsunobu reaction, and a late-stage C-H oxidation.

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