4.8 Article

Synthesis of rutaecarpine alkaloids via an electrochemical cross dehydrogenation coupling reaction

Journal

GREEN CHEMISTRY
Volume 21, Issue 20, Pages 5517-5520

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9gc03028j

Keywords

-

Funding

  1. National Natural Science Foundation of China [21861006]
  2. Guangxi Natural Science Foundation of China [2016GXNSFEA380001, 2018GXNSFBA281151]
  3. Guangxi Key RD Program [AB18221005]
  4. Science and Technology Major Project of Guangxi [AA17204058-21]
  5. Guangxi Science and Technology Base and Special Talents [guike AD19110027]
  6. State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources [CMEMR2019-A03]

Ask authors/readers for more resources

Substrates are directly oxidized at the anode without using any metal catalyst and oxidant to obtain a series of nitrogen heterocyclic compounds, including benzimidazoles and quinolinones. These compounds are highly tolerant to various functional groups and heterocycle-containing substrates. In addition, natural alkaloids, such as rutaecarpine and deoxyvasicinone, can be synthesized by this method.

Authors

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

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available