4.7 Article

Y Harnessing the reactivity of ortho-formyl-arylketones: base-promoted regiospecific synthesis of functionalized isoquinolines

Journal

CHEMICAL COMMUNICATIONS
Volume 55, Issue 57, Pages 8278-8281

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc03689j

Keywords

-

Funding

  1. SERB [EMR/2017/003218/OC]
  2. University of Delhi
  3. UGC
  4. CSIR

Ask authors/readers for more resources

An efficient and base-mediated one-pot regiospecific synthesis of structurally diversified isoquinolines and benzo[h] isoquinolines from easily accessible ortho-formyl-arylketones and aryl/(het)arylmethanamines has been described. Challenging 3-alkynyl/alkenyl isoquinolines and bis-isoquinolines were easily attained through this developed chemistry, which can be further used for various organic transformations. Operational simplicity, high atom-economy, broad substrate scope, functional group tolerance and applicability towards large scale synthesis are the advantageous features of this developed methodology.

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