Abstract
 Communication
 
Volume 82, Issue 1
Received, 1st July, 2010, Accepted, 27th July, 2010, Published online, 29th July, 2010.
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Enantioselective Synthesis of the C(2)-C(11) Cyclopropylfuran Segment of Pinnatin A
Masayoshi Tsubuki,* Terunobu Abekura, Kazunori Takahashi, and Toshio Honda*
Research Centre of Medicinal Sciences, Hoshi University, 2-4-41 Ebara, Shinagawa-ku, Tokyo 142-8501, Japan

Abstract
Synthesis of the C(2)-C(11) segment, cyclopropylfuran derivative, of pinnatin A was accomplished by Suzuki cross-coupling between chiral cyclopropylboronic acid and bromofuran as a key step. Addition of silver (I) oxide was found to promote the Suzuki cross-coupling reactions.

Graphical Abstract

Corresponding author; email: tsubuki@hoshi.ac.jp
   
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