4.7 Article

Cu-Catalyzed one-pot synthesis of thiochromeno-quinolinone and thiochromeno-thioflavone via oxidative double hetero Michael addition using in situ generated nucleophiles

Journal

CHEMICAL COMMUNICATIONS
Volume 56, Issue 62, Pages 8826-8829

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cc03210g

Keywords

-

Funding

  1. IIT Madras [CHY/17-18/847/RFIR/GSEK]
  2. CSIR, New Delhi

Ask authors/readers for more resources

A copper catalyzed three-component synthesis of pi-conjugated tetracyclic thiochromeno-quinolinone and thiochromeno-thioflavone was establishedviaoxidative double hetero Michael addition usingin situgenerated nucleophiles. Xanthate plays a dual role as an odourless sulfur source and a chemoselective reducing agent. Thein situformed iodine plays a crucial role in the oxidation step.

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