4.7 Review

Recent advances in Cu-catalyzed carbonylation with CO

Journal

ORGANIC CHEMISTRY FRONTIERS
Volume 9, Issue 23, Pages 6749-6765

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2qo01419j

Keywords

-

Funding

  1. National Natural Science Foundation of China [22061032]
  2. Natural Science Foundation of Inner Mongolia [2020MS02022]
  3. Science and Technology Program of Inner Mongolia [2020GG0134]
  4. State Key Laboratory of Bio-organic and Natural Products Chemistry of SIOC [21300-5206002]
  5. JUN-MA High-level Talents Program of Inner Mongolia University [21300-5185121]
  6. Grassland Talents Program of Inner Mongolia [12000-12102414]
  7. Highlevel Recruit Program of Inner Mongolia [12000-13000603]

Ask authors/readers for more resources

Transition metal-catalyzed carbonylation is a powerful and versatile strategy to synthesize complex carbonyl-containing molecules from simple feedstocks. Copper-catalyzed carbonylation using CO as the C(1) source has shown advantages of low cost and toxicity compared to noble metal catalysts. Recent advances in this field have summarized the conversion of easily accessible substrates into valuable carbonylated products, providing a greener alternative for catalytic carbonylation.
Transition metal-catalyzed carbonylation has emerged as a powerful and versatile strategy for the efficient construction of complicated carbonyl-containing molecules from simple chemical feedstocks in the past decades. Although many transition metals, especially noble metals, such as Ru, Rh, Pd, and others, have been applied successfully for these transformations, non-noble metal Cu-catalyzed carbonylation has shown a lot of advantages in terms of its low cost and toxicity. In this review, recent advances and contributions in Cu-catalyzed carbonylation using CO as the C(1) source were summarized. A variety of easily accessible substrates were converted into valuable carbonylated products including ketones, esters, amides and other products. The synthetic strategies described in this review provided an alternative greener option for catalytic carbonylation. Further studies and developments in this field would be inspired in the future.

Authors

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

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available