Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 85, Issue 19, Pages 12740-12746Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.0c00823
Keywords
-
Categories
Funding
- NIGMS-NIH [1R15GM126498-01]
- NSF MRI program [CHE:1726931]
- Northern Illinois University
Ask authors/readers for more resources
The conjugate addition reactions of trans-1,2-di(2-pyridyl)ethylene have been studied. This substrate reacts with organolithium nucleophiles, and the resulting anionic intermediates may be trapped by proton or various carbonyl-based electrophiles. It is suggested that the dipyridyl structure stabilizes the intermediate carbanion, allowing the Michael adduct to be captured by an added electrophile.
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
Share Paper
