Published March 16, 2009
| Accepted Version + Supplemental Material
Journal Article
Open
Catalytic Asymmetric Cycloaddition of Ketenes and Nitroso Compounds: Enantioselective Synthesis of α-Hydroxycarboxylic Acid Derivatives
- Creators
- Dochnahl, Maximilian
-
Fu, Gregory C.
Abstract
The appropriate choice of chiral catalyst and starting materials leads to the synthesis of 1,2‐oxazetidin‐3‐ones by cycloadditions of ketenes with nitroso compounds with very good regioselectivity and enantioselectivity. In addition to serving as potentially bioactive target molecules, the products can be transformed into other important classes of compounds, such as α‐hydroxycarboxylic acid derivatives.
Additional Information
© 2009 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim. Received: November 28, 2008; Published online: February 16, 2009. Support has been provided by the National Institutes of Health (National Institute of General Medical Sciences, grant R01-GM57034), the German Academic Exchange Service (postdoctoral fellowship for M.D.), Merck Research Laboratories, and Novartis.Attached Files
Accepted Version - nihms-102360.pdf
Supplemental Material - anie_200805805_sm_miscellaneous_information.pdf
Files
nihms-102360.pdf
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Additional details
- PMCID
- PMC2728616
- Eprint ID
- 103260
- Resolver ID
- CaltechAUTHORS:20200518-080028686
- NIH
- R01-GM57034
- Deutscher Akademischer Austauschdienst (DAAD)
- Merck Research Laboratories
- Novartis
- Created
-
2020-05-18Created from EPrint's datestamp field
- Updated
-
2021-11-16Created from EPrint's last_modified field