Synthesis of Disubstituted Oxindoles Using the Method of Asymmetric Cyanoamidation
2011-09-13
Loading...
View/Download File
Persistent link to this item
Statistics
View StatisticsJournal Title
Journal ISSN
Volume Title
Title
Synthesis of Disubstituted Oxindoles Using the Method of Asymmetric Cyanoamidation
Alternative title
Authors
Published Date
2011-09-13
Publisher
Type
Presentation
Abstract
Earlier studies demonstrate the ability of cyanoformamides to cyclize into 3,3-disubstituted oxindoles using chiral ligands, a palladium catalyst and Lewis base additives. Unknown, however, is the effect of chiral ligands and Lewis acids on the enantioselectivity of the same reaction. Studying these compounds should provide insight to their function in medicine or pharmaceuticals.
Description
Related to
Replaces
License
Series/Report Number
Funding information
Isbn identifier
Doi identifier
Previously Published Citation
Other identifiers
Suggested citation
Anand, Aarti; Douglas, Christopher. (2011). Synthesis of Disubstituted Oxindoles Using the Method of Asymmetric Cyanoamidation. Retrieved from the University Digital Conservancy, https://hdl.handle.net/11299/115476.
Content distributed via the University Digital Conservancy may be subject to additional license and use restrictions applied by the depositor. By using these files, users agree to the Terms of Use. Materials in the UDC may contain content that is disturbing and/or harmful. For more information, please see our statement on harmful content in digital repositories.