4.8 Article

Photoinduced Rearrangements of 3,3′-Bis(arylbenzofurans)

Journal

ORGANIC LETTERS
Volume 13, Issue 3, Pages 474-477

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol102816a

Keywords

-

Funding

  1. Roche Research Foundation
  2. Novartis Foundation
  3. Fonds der Chemischen Industrie

Ask authors/readers for more resources

Complex tetracyclic ring systems were assembled by a photoinduced rearrangement of 3,3'-bis(arylbenzofurans). Irradiation of 1 under N-2 atmosphere yielded the benzonaphthofurans 2 in 75-90% yield. When the reaction was conducted under an O-2 atmosphere in the presence of tetracyanoethylene (TCNE) a different reaction pathway was observed leading to the isolation of 3 as the major product. Also, the photochemical properties of these novel structures were investigated.

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