Journal
ORGANIC LETTERS
Volume 22, Issue 19, Pages 7604-7608Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.0c02805
Keywords
-
Categories
Funding
- NSFC [21572138]
- Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry, Sichuan Research Center for Drug Precision Industrial Technology
Ask authors/readers for more resources
An effective strategy to synthesize spirocyclic compounds, [imidazole-4,1'-indene], has been efficaciously developed relied on Rh(III)-catalyzed [3 + 2] spirocyclization of 2H-imidazoles and 1,3-diynes with excellent chemselectivity and regioselectivity. This protocol shows a straightforward way to construct the versatile spirocyclic compounds with wide functional group compatibility, high atom economy, and diverse functionalization of products.
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