4.7 Article

Dual gold/photoredox-catalyzed bis-arylative cyclization of chiral homopropargyl sulfonamides with diazonium salts: rapid access to enantioenriched 2,3-dihydropyrroles

Journal

CHEMICAL COMMUNICATIONS
Volume 53, Issue 51, Pages 6848-6851

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7cc03262e

Keywords

-

Funding

  1. National Natural Science Foundation of China [21622204, 21572186]
  2. Natural Science Foundation of Fujian Province for Distinguished Young Scholars [2015J06003]
  3. Qing Lan Project of Jiangsu Province
  4. Jiangsu University Foundation [13JDG059]
  5. NFFTBS [J1310024]

Ask authors/readers for more resources

A novel dual gold/photoredox-catalyzed bis-arylative cyclization of chiral homopropargyl sulfonamides with diazonium salts has been developed, allowing the facile synthesis of various enantioenriched 2,3-dihydropyrroles in generally moderate to good yields with excellent enantioselectivities under very mild conditions without using any strong oxidants. The reaction is proposed to undergo an Au-I/Au-III redox cycle promoted by visible-light photoredox catalysis.

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