Journal
CHEMICAL SCIENCE
Volume 11, Issue 6, Pages 1672-1676Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9sc06369b
Keywords
-
Categories
Funding
- National Research Foundation of Korea (NRF) - Korean government [NRF-2019R1A2C1087134, NRF-2019R1A4A2001440]
- GRRC Program of Gyeonggi Province [GRRCKyungHee2017-A01]
Ask authors/readers for more resources
A divergent cyclopropanation reaction has been accomplished via the dearomative addition of sulfur ylides to activated N-heteroarenes. A series of biologically significant molecular skeletons was obtained by the direct cyclopropanation of quinolinium zwitterions. Furthermore, a straightforward synthetic route to optically enriched cyclopropane-fused heterocycles was developed using sulfur ylides as chiral nucleophiles in the 1,4-dearomative reaction.
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