Journal
CHEMICAL COMMUNICATIONS
Volume 57, Issue 5, Pages 599-602Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cc06975b
Keywords
-
Categories
Funding
- EPSRC [EP/N025652/1] Funding Source: UKRI
Ask authors/readers for more resources
Regioselective and stereospecific directed C-H arylation of simple amine substrates, followed by cyclisation, resulted in the synthesis of 30 diverse, three-dimensional scaffolds. This unified approach significantly expanded the range of bridged ring systems containing both a nitrogen atom and an aromatic ring.
Regioselective and stereospecific directed C-H arylation of simple amine substrates, and cyclisation, delivered 30 diverse, three-dimensional scaffolds. The unified approach significantly expanded the range of bridged ring systems that contain both a nitrogen atom and an aromatic ring.
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