4.8 Article

Highly Enantioselective Synthesis of Multifunctionalized Dihydrofurans by Copper-Catalyzed Asymmetric [4+1] Cycloadditions of α-Benzylidene-β-ketoester with Diazo Compound

Journal

ACS CATALYSIS
Volume 3, Issue 4, Pages 685-688

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/cs400019u

Keywords

asymmetric; copper carbene; [4+1] cycloadditions; dihydrofurans

Funding

  1. National Natural Sciences Foundation of China [21121062, 20932008, 21272250]
  2. Major State Basic Research Development Program [2009CB825300]
  3. Chinese Academy of Sciences

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Highly efficient synthesis of chiral tetrasubstituted 2,3-dihydrofuran derivatives has been realized by Cu-catalyzed asymmetric [4 + 1] cycloadditions of alpha-benzylidene-beta-ketoester with a diazo compound. Following this methodology, a series of optically active multifunctionalized dihydrofurans were prepared in high yield with up to 96% ee and 99/1 dr.

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