Journal
CHEMICAL COMMUNICATIONS
Volume 46, Issue 37, Pages 6953-6955Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c0cc01522a
Keywords
-
Categories
Funding
- Spanish Ministry of Science and Innovation (MICINN) [AYA2009-13920-C02-02]
- Generalitat de Catalunya
- University of Bologna
- MICINN
- ICREA Funding Source: Custom
Ask authors/readers for more resources
The synthesis of Spiro compounds via a Michael-Michael-aldol reaction is reported. The reaction affords spirooxindole derivatives in good yields and in almost diastereo- and enantiopure form. Moreover, the reaction works with several heterocycles such as oxindoles, benzofuranones, pyrazolones or azlactones rendering the final Spiro compounds in good yields and excellent stereoselectivities.
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