4.4 Article

Synthesis of aryl [5]helicenes through Suzuki-Miyaura reaction and their optical properties

Journal

TETRAHEDRON
Volume 127, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2022.133075

Keywords

Arylation; Cross-coupling; 78-Dibromo [5]helicene; Palladium catalysis; Suzuki-Miyaura

Funding

  1. graduate research and innova-tion foundation of Chongqing of China
  2. National Natural Science Foundation of China
  3. Natural Science Foun-dation Project of CQ CSTC
  4. [CYS17018]
  5. [21372265]
  6. [21350110501]

Ask authors/readers for more resources

A series of arylated [5]helicenes were effectively obtained through palladium catalyzed Suzuki-Miyaura reaction under mild conditions. The optical properties of [5]helicene derivatives were studied and showed red-shift compared to [5]helicene. This Pd-catalyzed coupling provides an effective protocol for the synthesis of mono-/bisalkyl [5]helicenes.
A series of arylated [5]helicenes have been effectively obtained through palladium catalyzed Suzuki-Miyaura reaction, starting from 7,8-dibromo [5]helicene under mild conditions. Optical properties of [5]helicene derivatives were studied by UV-vis and fluorescence spectra, and both maximum absorption wavelength and emission wavelength showed red-shift compared with [5]helicene. This Pd-catalyzed coupling provides an effective protocol for synthesis of mono-/bisalkyl [5]helicenes.(c) 2022 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available