Published March 28, 2006
| Supplemental Material + Published + Cover Image
Journal Article
Open
2-Diazoacetoacetic acid, an efficient and convenient reagent for the synthesis of alpha-diazo-beta-ketoesters
Chicago
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Abstract
The formation of various alpha-diazo acetoacetic esters can be obtained in a single transformation with good to excellent yields using readily available 2-diazoacetoacetic acid.
Additional Information
© The Royal Society of Chemistry 2006 Received (in Bloomington, IN, USA) 13th December 2005, Accepted 27th January 2006. First published on the web 15th February 2006 The authors gratefully acknowledge the NSF (predoctoral fellowship for E.M.F.), Bristol-Myers Squibb (Graduate Fellowship in Synthetic Organic Chemistry to E.M.F.), AstraZeneca, Boehringer Ingelheim, Johnson & Johnson, Pfizer, Merck, Amgen, Research Corporation, Roche, the Dreyfus Foundation, and GlaxoSmithKline for generous funding. Electronic supplementary information (ESI) available: experimental details and characterization data for all compounds. See DOI: 10.1039/b517719gAttached Files
Published - MEYcc06.pdf
Supplemental Material - MEYcc05supp.pdf
Cover Image - MEYcc06diag.gif
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MEYcc05supp.pdf
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Additional details
- Eprint ID
- 3509
- Resolver ID
- CaltechAUTHORS:MEYcc06
- NSF Predoctoral Fellowship
- Bristol-Myers Squibb
- AstraZeneca
- Boehringer-Ingelheim
- Johnson and Johnson
- Pfizer
- Merck
- Amgen
- Research Corporation
- Roche
- Camille and Henry Dreyfus Foundation
- GlaxoSmithKline
- Created
-
2006-06-11Created from EPrint's datestamp field
- Updated
-
2021-11-08Created from EPrint's last_modified field