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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 28, 1998 - Issue 7
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Original Articles

Reactions of N-Phosphorylated Aziridines with Dianions Derived from Ethyl Acetoacetate and 1,3-Diketones: New Route to Substituted Pyrrolines and Pyrrolidines

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Pages 1127-1137 | Received 03 Nov 1997, Published online: 15 Aug 2006
 

Abstract

The nucleophilic ring-opening of N-(diethoxyphosphory)aziridines by the dianions derived from ethyl acetoacetate and 1,3-diketones has been studied. Acid-mediated cyclisation and dephosphorylation of the resulting products to a number of substituted pyrrolines and pyrrolidines has been also investigated.

Notes

References cited in ref. 3

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