Journal
ORGANIC CHEMISTRY FRONTIERS
Volume 6, Issue 3, Pages 388-392Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8qo01076e
Keywords
-
Categories
Funding
- National Natural Science Foundation of China [21871045, 21831002]
- Natural Science Foundation of the Jilin Province [20160519003JH, 20190201070JC]
- Changbai Mountain Scholarship Program
- Fundamental Research Funds for the Central Universities [2412017FZ014]
- Ten Thousand Talents Program
Ask authors/readers for more resources
We report that the Pd-0-catalyzed carboannulation of gamma,delta-alkenyl oximes with organohalides offers catalyst-controlled access to 5-membered cyclic nitrones or 6-membered cyclic oxime ethers. wherein substrate conformation can result in divergent reactivity, a phenomenon that likely arises from a shift in the mechanistic paradigm. The title transformation features a catalyst-controlled bond formation event that holds promise for the enantioselective synthesis of these important heterocycles.
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