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2-Diazoacetoacetic acid, an efficient and convenient reagent for the synthesis of alpha-diazo-beta-ketoesters

Meyer, Michael E. and Ferreira, Eric M. and Stoltz, Brian M. (2006) 2-Diazoacetoacetic acid, an efficient and convenient reagent for the synthesis of alpha-diazo-beta-ketoesters. Chemical Communications, 2006 (12). pp. 1316-1318. ISSN 1359-7345 http://resolver.caltech.edu/CaltechAUTHORS:MEYcc06

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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.


Item Type:Article
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/b517719g
Subject Keywords:C-H INSERTION; CARBONYL-COMPOUNDS; STEREOSELECTIVE-SYNTHESIS; CLAISEN REARRANGEMENT; WOLFF REARRANGEMENT; CYCLOADDITION; TRANSFORMATIONS; ACTIVATION; PRECURSORS; CATALYSTS
Record Number:CaltechAUTHORS:MEYcc06
Persistent URL:http://resolver.caltech.edu/CaltechAUTHORS:MEYcc06
Alternative URL:http://dx.doi.org/10.1039/b517719g
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:3509
Collection:CaltechAUTHORS
Deposited By: Archive Administrator
Deposited On:11 Jun 2006
Last Modified:26 Dec 2012 08:54

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