4.5 Article

Pd-Catalyzed Etherification of Nitroarenes

Journal

ORGANOMETALLICS
Volume 40, Issue 14, Pages 2209-2214

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.organomet.1c00183

Keywords

-

Funding

  1. JST CREST program [JPMJCR14L3]
  2. JSPS KAKENHI [JP15H05799]
  3. TOSOH corporation
  4. Japan Society for the Promotion of Science (JSPS)

Ask authors/readers for more resources

Through the use of a new designed ligand, Pd-catalyzed etherification of nitroarenes with arenols was achieved, allowing for the direct access to a range of unsymmetrical diaryl ethers. The design of the ligand facilitated both the oxidative addition and reductive elimination steps of the catalytic cycle, providing mechanistic insights for optimizing the reaction.
The Pd-catalyzed etherification of nitroarenes with arenols has been achieved using a new rationally designed ligand. Mechanistic insights were used to design the ligand so that both the oxidative addition and reductive elimination steps of a plausible catalytic cycle were facilitated. The catalytic system established here provides direct access to a range of unsymmetrical diary! ethers from nitroarenes.

Authors

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

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available