Ghorai, Manas K. ; Halder, Sandipan ; Samanta, Sauvik (2012) Regioselective Addition of 1,3-Dicarbonyl Dianions to Carbonyl Compounds: One Pot Lactonization and Ketalization of δ-Hydroxy-β-keto Esters to Protected Pyrone Derivatives Australian Journal of Chemistry, 65 (9). p. 1262. ISSN 0004-9425
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Official URL: http://doi.org/10.1071/CH12062
Related URL: http://dx.doi.org/10.1071/CH12062
Abstract
A simple and efficient strategy for the synthesis of 6-substituted-2-pyrone derivatives, by BF3·OEt2 mediated one pot cyclization and keto-protection of δ-hydroxy-β-keto esters, obtained via regioselective addition of 1,3-dicarbonyl dianion of ethyl acetoacetate to aldehydes and ketones is described.
Item Type: | Article |
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Source: | Copyright of this article belongs to CSIRO. |
ID Code: | 117117 |
Deposited On: | 15 Apr 2021 08:00 |
Last Modified: | 15 Apr 2021 08:00 |
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