4.8 Article

Synthesis of C60-Fused Tetrahydrocarbazole/Dibenzothiophene/Benzothiophene and Dibenzofuran Derivatives via Metal-Free Oxidative Dehydrogenative Carboannulation

Journal

ORGANIC LETTERS
Volume 18, Issue 16, Pages 4044-4047

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b01902

Keywords

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Funding

  1. NSFC [21302044, U1304524, 21372065, 21272057]
  2. China Postdoctoral Science Foundation [2015T80769, 2013M541981]
  3. Foundation and Frontier Technology Research of Henan Province [122300410296]
  4. Outstanding Youth Science Project Funding of Henan Normal University [14YQ004]

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A transition-metal-free oxidative dehydrogenative, coupling reaction has been developed for the direct construction of novel C-60-fused tetrahydrocarbazoles, dibenzothiophenes, benzothiophenes, and dibenzofurans. This new carboannulation reaction features high atom economy, operational simplicity, broad substrate scope, and excellent functional-group tolerance and provides a convenient access to a scarce class of fullerene derivatives.

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