4.5 Article

Accessing 2-Arylbenzofurans by CuI2(pip)2-Catalyzed Tandem Coupling/Cyclization Reaction: Mechanistic Studies and Application to the Synthesis of Stemofuran A and Moracin M

Journal

ASIAN JOURNAL OF ORGANIC CHEMISTRY
Volume 5, Issue 11, Pages 1345-1352

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ajoc.201600321

Keywords

benzofurans; copper; mechanistic studies; natural products; tandem reactions

Funding

  1. Fundamental Research Funds for the Central Universities [20720160047]
  2. NSFC [21273187, 21133004]

Ask authors/readers for more resources

An asymmetric dinuclear copper(I) complex, Cu-2(I)(pip)(2) (pip=(2-picolyliminomethyl)pyrrole anion), was used to catalyze the tandem coupling/cyclization reaction of o-iodophenols and terminal alkynes, which led to the formation of valuable 2-arylbenzofurans in good yields. DFT calculations showed that the two proximate copper atoms play cooperative roles throughout the catalytic cycle. Using this catalytic protocol, bioactive natural products stemofuran A and moracin M were concisely synthesized.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available