Journal
CHEMICAL COMMUNICATIONS
Volume 56, Issue 13, Pages 1948-1951Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cc00143k
Keywords
-
Categories
Funding
- National Natural Science Foundation of China [21703099, 2193044]
- Natural Science Foundation of Jiangsu Province for Youth [BK20170964]
- Nanjing Tech University [39837132, 39837123]
Ask authors/readers for more resources
An efficient [3+3] benzannulation of Morita-Baylis-Hillman carbonates with 1-indanylidenemalononitrile was achieved under metal-free reaction conditions selectively delivering a wide range of functional multi-substituted fluorene or fluorenone compounds in high yields, respectively (up to 86% yield). Moreover, experiments and quantum chemical calculations were also performed to study the mechanism of the transformation.
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