Journal
CHEMICAL SCIENCE
Volume 3, Issue 1, Pages 53-57Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c1sc00621e
Keywords
-
Categories
Funding
- National Institute of General Medical Science [R01GM73072]
- Northwestern University
- Organic Syntheses/Organic Reactions
Ask authors/readers for more resources
Lewis acid activation with N-heterocyclic carbene (NHC) catalysis has presented new opportunities for enantioselective reaction development. Recent findings illustrate that Lewis acids can play an important role in homoenolate annulations by: enhancement of the reactivity, reversal of the diastereo-or regioselectivity, and activation of previously inactive electrophiles. Additionally, the incorporation of a Lewis acid into Bronsted base-catalyzed conjugate addition allowed for an increase in yields.
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