4.8 Article

Room Temperature Cu-Catalyzed N-Arylation of Oxazolidinones and Amides with (Hetero)Aryl Iodides

Journal

ORGANIC LETTERS
Volume 24, Issue 5, Pages 1253-1257

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.2c00122

Keywords

-

Funding

  1. Chinese Academy of Sciences [XDB20020200, QYZDJ-SSW-SLH029]
  2. National Natural Science Foundation of China [21621002, 21831009, 21991110]
  3. CAS Presidents International Fellowship Initiative (PIFI)

Ask authors/readers for more resources

BPMO is an appropriate promoter for the Cu-catalyzed N-arylation reaction at room temperature, showing excellent chemoselectivity between aryl iodides and aryl bromides, and good tolerance towards diverse functional groups.
N,N & PRIME;-Bis(pyridin-2-ylmethyl)oxalamide (BPMO) was found to be an apposite promoter for the Cu-catalyzed N-arylation of oxazolidinones and primary and secondary amides with (hetero)aryl iodides at room temperature. Excellent chemoselectivity reached between aryl iodides and aryl bromides, and a wide range of functional groups tolerated the reaction conditions, which led to the formation of greatly diverse N-arylation products.

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