Journal
ORGANIC CHEMISTRY FRONTIERS
Volume 6, Issue 8, Pages 1118-1122Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9qo00045c
Keywords
-
Categories
Funding
- NSFC [21871096, 21672071]
- Ministry of Science and Technology of the People's Republic of China [2016YFA0602900]
- NSF of Guangdong [2018B030308007, 2018A030310359, 2016A030310433]
- China Postdoctoral Science Foundation [2018M633042, 2018M643062]
Ask authors/readers for more resources
A new method for the synthesis of furan-/benzo-fused fluorenes through copper(i)-catalyzed coupling of conjugated enynones or -diazocarbonyl compounds with dialkynylbenzenes has been developed. This process includes 5-exo-dig cyclization, carbene migratory insertion, Schmittel cyclization and 1,5-H transfer. The obvious advantages of wide substrate scopes, mild reaction conditions, and high atom efficiency make this system highly appealing for the construction of six-substituted benzofuran-embedded fluorenes in a one-pot manner.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available