4.8 Article

Palladium-Catalyzed Highly Diastereoselective Oxidative Cascade Cyclization Reactions

Journal

ORGANIC LETTERS
Volume 11, Issue 9, Pages 1911-1914

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol900355h

Keywords

-

Funding

  1. University of Hong Kong
  2. Hong Kong Research Grants Council [HKU 705807P]

Ask authors/readers for more resources

Isoquinoline and quinoline have been discovered as novel ligands for palladium-catalyzed oxidative cascade cyclization reactions. With our new catalyst systems (Pd(OAc)(2)/disoquinoline or quinoline), unsaturated anilides cyclize under an oxygen atmosphere (1 atm) to furnish structurally versatile indoline derivatives in good yields. One C-N bond and two C-C bonds are formed in a single step with excellent diastereoselectivities (dr > 24:1).

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